Desaturases of a green microalga and uses thereof

ABSTRACT

Isolated proteins which are at least partially encoded by polynucleotide sequences encoding novel desaturases are provided together with a composition which includes these isolated proteins. A transgenic plant, a transgenic alga, or a transgenic seed transformed by the polynucleotides encoding proteins which are at least partially encoded by novel desaturases are also provided. The invention also includes a process for making a very long-chain polyunsaturated fatty acid in a transformed cell, a transgenic alga, or a transgenic plant expressing the isolated protein or proteins which are at least partially encoded by the polynucleotide sequences encoding novel Δ5, Δ6, or Δ12 desaturases.

FIELD OF INVENTION

This invention is directed to, inter alia, proteins having Δ2, Δ6, or Δ5 desaturase activity, isolated DNA molecules encoding the same, and methods of making and utilizing the same.

BACKGROUND OF THE INVENTION

Very long-chain polyunsaturated fatty acids (VLC-PUFA) of 20 or 22 carbon atoms are indispensable components of human nutrition. They are necessary for normal life-long physiology and benefit the well-being of the human body. Nutritionally important VLC-PUFAs include the ω3-fatty acids, eicosapentaenoic acid (EPA, 20:5ω3) and docosahexaenoic acid (DHA, 22:6ω3) and the ω6-fatty acid, arachidonic acid (ARA, 20:4ω6) and dihomo-y-linolenic acid (DGLA, 20:3ω6) which are the major components of membrane phospholipids of the retina, brain and testis. ARA and DHA are the predominant fatty acids in the human brain and breast milk. ARA is necessary for normal fetal growth, and cognitive development in infants. Many studies highly suggested supplementation of infant formula with DHA and ARA. Besides the structural function in membranes, ARA is the primary substrate in eicosanoids biosynthesis which regulates many physiological processes such as homeostasis, reproduction, immune and inflammatory responses.

Microalgae are the most efficient producers and one of the richest sources of VLC-PUFAs. Furthermore, algae can be used as sources of genes for the implementation of VLC-PUFA biosynthesis in genetically engineered oil crops. The genetic information on enzymes involved in the biosynthesis of VLC-PUFA in some algae led to in vivo applications of VLC-PUFA production in seed oil. The gene pool of the green freshwater microalga Parietochloris incisa (Trebouxiophyceae) is of special interest since it is the only known microalga able to accumulate extraordinary high amounts of ARA-rich triacylglycerols (TAG). When P. incisa is cultivated under nitrogen starvation, the condition triggering storage oil accumulation, ARA constitutes about 60 percent of total fatty acids (TFA) and over 95 percent of cellular ARA is deposited in TAG in cytoplasmic lipid bodies.

The biosynthesis of VLC-PUFA in microalgae follows two major pathways, designated as ω6 and ω3. In these pathways, linoleic acid (LA; 18:2ω6) and α-linolenic acid (ALA; 18:3ω3) go through sequential, Δ6 desaturation, Δ6 elongation and Δ5 desaturation, yielding ARA and EPA, respectively. E.g., in the red microalga Porphyridium cruentum and the green microalga P. incisa, oleic acid (18:1) is first desaturated to LA and γ-linolenic acid (GLA, 18:3ω6) through Δ12 and Δ6 desaturations, followed by elongation to 20:3ω6 and Δ5 desaturation to yield ARA via the ω6 pathway. In P. incisa, the extraplastidial lipids, phosphatidylcholine (PC) and the betaine lipid, diacylglyceroltrimethylhomoserine (DGTS), are involved in the Δ12 and, subsequently, the Δ6 desaturations, whereas phosphatidylethanolamine (PE) along with PC are the suggested major substrates for the Δ5 desaturation of 20:3ω6 to 20:4ω6. The same enzymes are involved in the biosynthesis of VLC-PUFA through the ω3 pathway in the green microalga Ostreococcus tauri.

VLC-PUFAs may also be generated by an alternative Δ8 desaturation pathway. E.g., in the marine haptophyte Isocrysis galbana and in the fresh water euglenophyte Euglena gracilis, where LA and ALA are first elongated by C18 Δ9-specific fatty acid elongase followed by sequential Δ8 and AS desaturations to ARA, DGLA or EPA. The extraplastidial Δ12 desaturase is an integral ER-bound protein which is responsible for the desaturation of oleic acid and production of LA, mainly on phosphatidylcholine (PC). Δ5 and Δ6 desaturases contain a fused cytochrome b5 domain in their N-terminus, serving as an electron donor, and introduce a double bond at a site closer to the carboxyl group than any of the pre-existing double bonds in the substrate fatty acid, thereby called ‘front-end’ desaturases. Desaturases with Δ6 or Δ5 activity have been isolated from various organisms, e.g., the nematode C. elegans, the fungus Mortierella alpina, the moss Physcomitrella patens, the liverwort Marchantia polymorpha and the algae Phaeodactylum tricornutum, Thalassiosira pseudonana and Ostreococcus tauri. Some of these desaturases have been introduced together with PUFA-specific elongases into constructs for transformation of yeast and oil seed plants to reconstitute VLC-PUFA biosynthesis in the heterologous organisms.

SUMMARY OF THE INVENTION

In one embodiment, the present invention provides an isolated protein comprising, an amino acid sequence set forth in SEQ ID NO: 1.

In another embodiment, the present invention further provides an isolated protein comprising, an amino acid sequence set forth in SEQ ID NO: 2.

In another embodiment, the present invention further provides an isolated protein comprising, an amino acid sequence set forth in SEQ ID NO: 3.

In another embodiment, the present invention further provides a composition comprising a protein comprising, an amino acid sequence set forth in SEQ ID NO: 1, a composition comprising a protein comprising, an amino acid sequence set forth in SEQ ID NO: 2, a composition comprising a protein comprising, an amino acid sequence set forth in SEQ ID NO: 3, or a composition comprising any combination thereof.

In another embodiment, the present invention further provides a transgenic plant, a transgenic seed, a transformed cell, or a transgenic alga transformed by a polynucleotide encoding: (1) a protein comprising, an amino acid sequence set forth in SEQ ID NO: 1, (2) a protein comprising, an amino acid sequence set forth in SEQ ID NO: 2, (3) a protein comprising, an amino acid sequence set forth in SEQ ID NO: 3, or a transgenic plant, a transgenic seed, or a transgenic alga transformed by any combination of the polynucleotides (1), (2), and (3).

In another embodiment, the present invention further provides a method of producing very long-chain polyunsaturated fatty acid (VLC-PUFA) in a plant, a plant cell, or an alga comprising the step of transforming a plant, an alga, or a plant cell with a polynucleotide encoding: (1) a protein comprising, an amino acid sequence set forth in SEQ ID NO: 1, (2) a protein comprising, an amino acid sequence set forth in SEQ ID NO: 2, (3) a protein comprising, an amino acid sequence set forth in SEQ ID NO: 3, or transforming a plant, a plant cell, or an alga with any combination of the polynucleotides (1), (2), and (3), thereby producing a VLC-PUFA in a plant, a plant cell, or an alga.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1. Depicts the deduced amino acid sequences of P. incisa PiDes12 (A), PiDes6 (B), and PiDes5 (C) are aligned with their closest homologs using CLUSTAL W (1.83) multiple sequence alignment program (default). Conserved motifs characteristic of each desaturase sequence are highlighted. GeneBank accession numbers for the sequences are: A) C. reinhardtii (XP 001691669); C. vulgaris (BAB78716), G. hirsutum (AAL37484), S. oleracea (BAC22091), O. europaea (AAW63040). B) M. polymorpha (AAT85661), P. tricornutum (AAL92563), T. pseudonana (AAX14505), O. tauri (AAW70159), M. squamata (CAQ30479). C) O. tauri (CAL57370), M. squamata (CAQ30478), M. polymorpha (AAT85663), D. discoideum (BAA37090), M. alpina (AAC72755), P. tricornutum (AY082392).

FIG. 2. Is an unrooted phylogram of PiDes12, PiDes6, PiDes5 and some functionally characterized Δ12, Δ6 and Δ5 desaturases (vertebrate and invertebrate desaturases are not included). The alignment was generated by the CLUSTAL W program and the unrooted phylogram was constructed in the neighbor-joining method using the MEGA4 software [47]. GeneBank sources of the sequences are: BAB78716 (Δ12, Chlorella vulgaris), XP_(—)001691669 (Δ12, C. reinhardtii), BAC22091 (Δ12, Spinacia oleracea), AAL37484 (Δ12, Gossypium hirsutum), AAW63040 (Δ12, Olea europaea), CAB94993 (Δ6, Ceratodon purpureus), AAT85661 (Δ6, M. polymorpha), BAΔ85588 (Δ6, M. alpina), AAL92563 (Δ6, P. tricornutum), AAX14505 (Δ6, T. pseudonana), (Δ6, Pythium irregulare), CAL57370 (Δ5, O. tauri), AAT85663 (Δ5, M. polymorpha), AAL13311 (Δ5, P. irregulare), CAD53323 (Δ5, Phytophthora megasperma), BAΔ37090 (Δ5, Dictyostelium discoideum), AAC72755 (Δ5, M. alpina), CAQ30478 (Δ5, M. squamata), CAQ30479 (Δ6, M. squamata), AAW70159 (Δ6, O. tauri), CS020055 (Δ5, P. patens).

FIG. 3. Provides graphs representing GC FAMEs of recombinant yeast harboring pYES2 (control), pY PiDes6 (A) fed with 18:2 or 18:3ω3, and pYPiDes5 (B) fed with 20:3ω6, 20:4ω3 or 18:1.

FIG. 4. Is a graph showing the changes in expression of the PiDes12, PiDes6, and PiDes5 genes under N-starvation and ARA percent share in total fatty acids. The transcript abundance of the genes was normalized to that of the actin gene.

FIG. 5. Depicts the amino acid sequence of P. incisa PiELO1 aligned with its closest homologs using CLUSTAL W (1.83) multiple sequence alignment program (default). Conserved motifs characteristic of PUFA elongase sequences are highlighted. GeneBank accession numbers for the sequences are OtELO1 (O. tauri, AAV67797), MpELO1 (M. polymorpha, AAT85662), PpELO1 (P. patens, AAL84174), MpELO2 (M. polymorpha, BAE71129), and ThrELO1 Thraustochytrium sp. FIN-10, ABC18313).

FIG. 6. Is a hydropathy plot of the amino acid sequence of PiELO1. The lower dashed line and the upper line represent the loose transmembrane region cutoff and the strict transmembrane region cutoff, respectively.

FIG. 7. Is an unrooted phylogram of PiELO1 and some other functionally characterized PUFA elongases. The alignment was generated by the CLUSTAL W program and the unrooted phylogram was constructed by the neighbor-joining method using the MEGA4 software. GeneBank accession numbers for the PUFA elongases are: ACK99719 (Δ6, P. incisa), AAV67797 (Δ6, O. tauri), AAV67798 (Δ5, O. tauri), AAT85662 (Δ6, M. polymorpha), BAE71129 (Δ5, M. polymorpha), AAL84174 (Δ6, P. patens), CAJ 30819 (Δ6, Thraustochytrium sp.), CAM55873 (Δ5, Thraustochytrium sp.), AAF70417 (Δ6, M. alpina), XP_(—)001467802 (L. infantum), AAV67803 (Δ6/Δ5, O. mykiss), NP_(—)001029014 (Δ6/Δ5, C. intestinalis), NP_(—)068586 (Δ6/Δ5, H. sapiens), AAY15135 (Δ5, P. salina), CAM55851 (Δ6 P. tricornutum), AAL37626 (Δ9, I. galbana), AAV67799 (Δ6, T. pseudonana), AAV67800 (Δ5, T. pseudonana), CAΔ92958 (Δ6, C. elegans), NP _(—)599209 (Δ6/Δ5, R. norvegicus).

FIG. 8. Is a GC plot of FAMES of recombinant yeast harboring pYES2 and PiELO1 fed with 18:3ω6 (A) and 18:4ω3 (B) CONTROL.

FIG. 9. Is a bar graph summarizing the results of quantitative Real-time RT-PCR analysis of PiELO1 gene expression in log phase (Time 0) and N-starved (3, 7 & 14 d) cells of P. incisa. The transcript abundance of the gene was normalized to 18S SSU rRNA gene.

DETAILED DESCRIPTION OF THE INVENTION

In one embodiment, the present invention provides an isolated protein. In another embodiment, the present invention provides that the isolated protein is a polypeptide. In another embodiment, the present invention provides that the isolated protein is an enzyme. In another embodiment, the present invention provides that the isolated protein is a desaturase. In another embodiment, the present invention provides that the isolated protein is an algal desaturase. In another embodiment, the present invention provides that the isolated protein is a microalgae desaturase. In another embodiment, the present invention provides that the isolated protein is a

Δ12 desaturase. In another embodiment, the present invention provides that the isolated protein is a Δ6 desaturase. In another embodiment, the present invention provides that the isolated protein is a Δ5 desaturase. In another embodiment, the present invention provides that the isolated protein is a microalgae desaturase produced in a plant cell. In another embodiment, the present invention provides that the isolated protein is a microalgae desaturase produced in an algal cell.

In another embodiment, the present invention provides a Δ12 desaturase comprising the amino acid sequence:

(SEQ ID NO: 1) MGKGGCYQAGPPSAKKWESRVPTAKPEFTIGTLRKAIPVHCFERSIPRSF AYLAADLAAIAVMYYLSTFIDHPAVPRVLAWGLLWPAYWYFQGAVATGVW VIAHECGHQAFSPYQWLNDAVGLVLHSCLLVPYYSWKHSHRRHHSNTGST TKDEVFVPREAAMVESDFSLMQTAPARFLVIFVSLTAGWPAYLFANASGR KYGKWANHFDPYSPIFTKRERSEIVVSDVALTVVIAGLYSLGKAFGWAWL VKEYVIPYLIVNMWLVMITLLQHTHPELPHYADKEWDWLRGALATCDRSY GGMPDHLHHHIADTHVAHHLFSTMPHYHAQEATEAIKPILGKYYKQDKRN VWAALWEDFSLCRYVAPDTAGSGILWFRA.

In another embodiment, the present invention provides a Δ6 desaturase comprising the amino acid sequence:

(SEQ ID NO: 2) MCQGQAVQGLRRRSSFLKLTGDAIKGAVAAISDFNKLPAATPVFARRSLS DSALQQRDGPRSKQQVTLEELAQHNTPEDCWLVIKNKVYDVSGWGPQHPG GHVIYTYAGKDATDVFACFHAQTTWSQLRPFCIGDIVEEEPMPALLKDFR ELRTRLQQQGLFRSNKLYYLYKVASTLSLLAAALAVLITQRDSWLGLVGG AFLLGLFWQQSGWLAHDFLHHQVFTDRQWNNVMGYFLGNVCQGFSTDWWK SKHNVHHAVPNELDSDSKAARDPDIDTLPLLAWSSEMLDSMSNSGARLFV RMQHYFFFPILLFARMSWCQQSVAHASDLSRTSKAGVYELAYLALHYAWF LGAAFSVLPPLKAVVFALLSQMFSGFLLSIVFVQSHNGMEVYSDTKDFVT AQIVSTRDILSNVWNDWFTGGLNYQIEHHLFPTLPRHNLGKVQKSIMELC HKHGLVYENCGMATGTYRVLQRLANVAAEA.

In another embodiment, the present invention provides a AS desaturase comprising the amino acid sequence:

(SEQ ID NO: 3) MMAVTEGAGGVTAEVGLHKRSSQPRPAAPRSKLFTLDEVAKHDSPTDCWV VIRRRVYDVTAWVPQHPGGNLIFVKAGRDCTQLFDSYHPLSARAVLDKFY IGEVDVRPGDEQFLVAFEEDTEEGQFYTVLKKRVEKYFRENKLNPRATGA MYAKSLTILAGLALSFYGTFFAFSSAPASLLSAVLLGICMAEVGVSIMHD ANHGAFARNTWASHALGATLDIVGASSFMWRQQHVVGHHAYTNVDGQDPD LRVKDPDVRRVTKFQPQQSYQAYQHIYLAFLYGLLAIKSVLLDDFMALSS GAIGSVKVAKLTPGEKLVFWGGKALWLGYFVLLPVVKSRHSWPLLAACWL LSEFVTGWMLAFMFQVAHVTSDVSYLEADKTGKVPRGWAAAQAATTADFA HGSWFWTQISGGLNYQVVHHLFPGICHLHYPAIAPIVLDTCKEFNVPYHV YPTFVRALAAHFKHLKDMGAPTAIPSLATVG.

In another embodiment, the desaturase of the present invention comprises an amino acid sequence that is at least 60% homologous to the amino acid sequence of SEQ ID NO: 1, SEQ ID NO: 2, or SEQ ID NO: 3. In another embodiment, the desaturase comprises an amino acid sequence that is at least 70% homologous to the amino acid sequence of SEQ ID NO: 1, SEQ NO: 2, or SEQ ID NO: 3. In another embodiment, the desaturase comprises an amino acid sequence that is at least 75% homologous to the amino acid sequence of SEQ ID NO: 1, SEQ ID NO: 2, or SEQ ID NO: 3. In another embodiment, the desaturase comprises an amino acid sequence that is at least 80% homologous to the amino acid sequence of SEQ ID NO: 1, SEQ ID NO: 2, or SEQ ID NO: 3. In another embodiment, the desaturase comprises an amino acid sequence that is at least 85% homologous to the amino acid sequence of SEQ ID NO: 1, SEQ ID NO: 2, or SEQ ID NO: 3. In another embodiment, the desaturase comprises an amino acid sequence that is at least 90% homologous to the amino acid sequence of SEQ ID NO: 1, SEQ ID

NO: 2, or SEQ ID NO: 3. In another embodiment, the desaturase comprises an amino acid sequence that is at least 95% homologous to the amino acid sequence of SEQ ID NO: 1, SEQ ID NO: 2, or SEQ ID NO: 3. In another embodiment, the desaturase comprises an amino acid sequence that is at least 98% homologous to the amino acid sequence of SEQ ID NO: 1, SEQ ID NO: 2, or SEQ ID NO: 3.

In another embodiment, the desaturase of the present invention comprises an amino acid sequence that is at least 60% identical to the amino acid sequence of SEQ ID NO: 1, SEQ ID NO: 2, or SEQ ID NO: 3. In another embodiment, the desaturase comprises an amino acid sequence that is at least 70% identical to the amino acid sequence of SEQ ID NO: 1, SEQ ID NO: 2, or SEQ ID NO: 3. In another embodiment, the desaturase comprises an amino acid sequence that is at least 75% identical to the amino acid sequence of SEQ ID NO: 1, SEQ ID NO: 2, or SEQ ID NO: 3. In another embodiment, the desaturase comprises an amino acid sequence that is at least 80% identical to the amino acid sequence of SEQ ID NO: 1, SEQ ID NO: 2, or SEQ ID NO: 3. In another embodiment, the desaturase comprises an amino acid sequence that is at least 85% identical to the amino acid sequence of SEQ ID NO: 1, SEQ ID NO: 2, or SEQ ID NO: 3. In another embodiment, the desaturase comprises an amino acid sequence that is at least 90% identical to the amino acid sequence of SEQ ID NO: 1, SEQ ID NO: 2, or SEQ ID NO: 3. In another embodiment, the desaturase comprises an amino acid sequence that is at least 95% identical to the amino acid sequence of SEQ ID NO: 1, SEQ ID NO: 2, or SEQ ID NO: 3. In another embodiment, the desaturase comprises an amino acid sequence that is at least 98% identical to the amino acid sequence of SEQ ID NO: 1, SEQ ID NO: 2, or SEQ ID NO: 3.

In another embodiment, the desaturase as described herein comprises at least a portion of the amino acid shown in SEQ ID. NO: 1, SEQ ID NO: 2, or SEQ ID NO: 3. In another embodiment, the desaturase as described herein is a variant of SEQ ID. NO: 1, SEQ ID NO: 2, or SEQ ID NO: 3. In another embodiment, the term “variant” in relation to a certain sequence means a protein or a polypeptide which is derived from the sequence through the insertion or deletion of one or more amino acid residues or the substitution of one or more amino acid residues with amino acid residues having similar properties, e.g., the replacement of a polar amino acid residue with another polar amino acid residue, or the replacement of a non-polar amino acid residue with another non-polar amino acid residue. In all cases, variants must have a desaturase function as defined herein.

In another embodiment, the desaturase as described herein further comprises a leader peptide. In another embodiment, the leader peptide allows the polypeptide to be specifically located or targeted to a target organelle within the cell. In another embodiment, the desaturase as described herein further comprises a sequence motif responsible for microsomal localization. In another embodiment, a desaturase as described herein further comprises chemical modification such as glycosylation that increases its stability. In another embodiment, a desaturase as described herein further comprises a peptide unrelated to desaturase which increases its stability.

In another embodiment, the present invention provides an isolated PUFA desaturase. In another embodiment, the present invention provides an isolated polypeptide comprising a functional long chain polyunsaturated fatty acid (PUFA) desaturase. In another embodiment, the present invention provides that the polypeptide has the function of desaturating a chain longer than 18 carbons fatty acid. In another embodiment, the present invention provides that the polypeptide has the function of desaturating a chain longer than 20 carbons fatty acid.

In another embodiment, the present invention provides an isolated PUFA desaturase comprising a fused N-terminal cytochrome b5 domain. In another embodiment, the present invention provides an isolated PUFA desaturase which desaturates ω6 substrates. In another embodiment, the present invention provides an isolated PUFA desaturase which desaturates both ω3 substrates. In another embodiment, the present invention provides an isolated PUFA desaturase which desaturates both ω3 and ω6 substrates. In another embodiment, the present invention provides an isolated PUFA desaturase encoded by SEQ ID NO: 1 (PiDes12 or Δ12). In another embodiment, the present invention provides an isolated PUFA desaturase encoded by SEQ ID NO: 2 (PiDes6 or Δ6). In another embodiment, the present invention provides an isolated PUFA desaturase encoded by SEQ ID NO: 3 (PiDes5 or Δ5). In another embodiment, the substrate for the present invention isolated PUFA desaturase is 18:2ω6, 20:3ω6, 20:4ω3, and 20:3ω3

In another embodiment, the present invention provides an isolated PUFA desaturase which desaturates 20:3ω3 to a non-methylene-interrupted 20:4^(Δ5). In another embodiment, the present invention provides that PiDes5 desaturates 20:3ω3 to a non-methylene-interrupted 20:4^(Δ5). In another embodiment, the present invention provides that PiDes5 converts 20:4ω3 into the respective Δ5 product, 20:5ω3 (EPA) as well as the added 18:1 into the non-methylene-interrupted 18:2^(Δ5, 9).

In another embodiment, the present invention provides a protein comprising a desaturase activity. In another embodiment, the present invention provides a protein consisting a desaturase activity. In another embodiment, the present invention provides that the protein of the invention is a recombinant desaturase. In another embodiment, the present invention provides that the desaturase is a polyunsaturated fatty acid (PUFA)-specific desaturase. In another embodiment, the present invention provides that the desaturase desaturates precursors of arachidonic acid. In another embodiment, the present invention provides that the desaturase desaturates precursors of EPA. In another embodiment, the present invention provides that the desaturase desaturates immediate precursors of arachidonic acid (ARA). In another embodiment, the present invention provides that the protein as described herein is used to elevate PUFA levels in animals, thereby providing a ready source of PUFAs.

In another embodiment, the expression and/or transcription of the desaturase as described herein is up-regulated during nitrogen starvation. In another embodiment, the expression and/or transcription of the desaturase as described herein is up-regulated under oleogenic conditions. In another embodiment, oleogenic conditions comprise the presence of a Δ6 substrate for Δ6 or Δ5 fatty acid desaturase. In another embodiment, oleogenic conditions comprise 18:2ω6 and 20:3ω6. In another embodiment, oleogenic conditions comprise nitrogen starvation. In another embodiment, the expression and/or transcription level of the desaturases as described herein correlates with the production of ARA precursors. In another embodiment, oleogenic conditions comprise nitrogen starvation. In another embodiment, the expression and/or transcription level of the desaturases as described herein correlates with the production of DGLA precursors, EPA precursors, DHA precursors, ARA precursors, or any combination thereof.

In another embodiment, the present invention provides an isolated polynucleotide encoding the protein as described herein. In another embodiment, an isolated polynucleotide is an isolated DNA molecule. In another embodiment, an isolated polynucleotide is an isolated cDNA molecule. In another embodiment, the isolated polynucleotide comprises a sequence encoding the protein as described herein. In another embodiment, the isolated polynucleotide comprises a DNA sequence encoding a desaturase as described herein. In another embodiment, the isolated polynucleotide comprises a DNA sequence encoding a polypeptide comprising a desaturase activity. In another embodiment, the isolated polynucleotide comprises a DNA sequence encoding a polypeptide consisting a desaturase activity.

In another embodiment, the isolated polynucleotide comprises a DNA sequence comprising the sequence:

(SEQ ID NO: 4, PiDes12) atggggaaaggaggctgttaccaggccgggcctcctagcgcaaagaaatg ggagagtagggtgcccactgccaaacccgagttcacgatcggaaccctcc gcaaagctataccggtccactgcttcgaacggtccatccctcggtcattg cctaccttgcggcagacctggcggctattgcggtcatgtactacctgagc actttcatcgatcatcccgccgtgccgcgggtcctggcctggggtttgct gtggcctgcctactggtacttccaaggtgctgtggcgacaggcgtctggg tgattgctcacgagtgcggccaccaggcgttctcgccctaccagtggctc aacgacgctgtggggcttgtgctgcactcctgcttgctggtgccctatta ctcctggaagcactcacacagacggcaccactccaacaccggaagcacca ccaaggatgaggtgtttgtcccccgggaagcagccatggtggagtcggac ttctccttgatgcagacagctcccgcgcggttcctggtcatcttcgtctc gctgaccgctggctggcctgcctacctgtttgccaatgcatctggccgca agtatggcaagtgggccaaccactttgacccctactcacccatcttcacc aagcgcgagcgcagcgagatcgttgtcagcgatgtcgcgctgacggtggt catcgcggggctctactcgctgggcaaggcgtttggctgggcctggctgg tcaaggagtatgtgatcccctacctcatcgtcaacatgtggctggtcatg atcacgctgctgcagcacacgcaccccgagctgccgcactacgccgacaa ggagtgggactggctgcgcggcgcgctggccacctgcgatcgcagctacg gcggcatgccggaccacctgcaccaccacatcgccgacacgcacgtcgct caccacctgttctccaccatgccgcactaccatgcgcaggaggcgactga ggcgatcaagcccatcctgggcaagtactacaagcaggacaagcgcaacg tctgggcagcgctctgggaggatttcagcctgtgccgctatgtggcgcct gacacagcaggctcgggcatcctgtggttccgcgcttga. In another embodiment, SEQ ID NO: 4 encodes the amino acid sequence of SEQ ID NO: 1.

In another embodiment, the isolated polynucleotide comprises a DNA sequence comprising the sequence:

(SEQ ID NO: 5, PiDes6) atgtgccagggacaggcagtccagggtctgaggcgccggagttcattatg aagctcaccggggacgctatcaaaggggccgttgccgcaatatcagactt caacaagctcccggccgcaacgccagtgttcgccaggcggtcactttccg acagcgctctgcagcagcgagatggcccgcgcagcaagcagcaggtcacc ctggaagagctagcgcagcataatacgcctgaggattgctggctggtcat caagaacaaggtgtacgacgtcagcggttggggaccgcagcaccccggtg ggcacgtgatctatacgtatgctggcaaagacgccacggacgtttttgcc tgatccatgcccagaccacttggtcgcagttgagacccttctgcatcggg gacattgtggaggaggagccaatgccggcgctgctcaaagacttccgcga gctgcgcacccggctgcagcagcagggcctgtttcgcagcaacaagagta ctacagtacaaggtggccagcacgctgagcctactggcggccgcgctggc agtgctgatcacgcagcgcgactcctggctgggtctcgtcggcggcgcgt tcctgctgggcctcttaggcagcagtcgggctggctggcgcacgacttcc tgcaccaccaggtcttcaccgaccgccagtggaacaacgtgatgggctac ttcctgggcaacgtctgccagggcttcagcacggactggtggaagagcaa gcacaacgtgcaccacgcggtgcccaacgagctcgacagcgacagcaagg cggcgcgggaccccgacatcgacacgctgcccctgctggcctggagctcg gagatgctggacagcatgagcaactcgggcgcgcgcctgtttgtgcgcat gcagcactacttcttcttccccatcctgctcttcgcgcgcatgtcctggt gccagcagtctgtcgcgcacgcctcggacctgtccaggacctcaaaggcg ggcgtgtatgagctggcgtatcttgcgctgcattatgcctggttcctggg cgcggccttcagcgtgctcccgcccctcaaggcggtcgtgttcgcgctgc tcagccagatgttttccggcttcctgctctccatcgtctttgtgcagagc cacaacggcatggaggtgtacagcgacacaaaggactttgtgacggccca gattgtgtccacgcgcgacatattgtcaaacgtctggaacgactggttca caggcgggctgaactaccagatcgagcaccacctgttccccacgctgccg cgccacaacctgggcaaggtccagaagtccatcatggagctgtgccacaa gcatggcctggtgtacgaaaactgcggcatggctactggcacctatcgtg tgctgcagcgcctggcaaacgtggcagctgaggcctag. In another embodiment. SEQ ID NO; 5 encodes the amino acid sequence of SEQ ID NO: 2.

In another embodiment, the isolated polynucleotide comprises a DNA sequence comprising the sequence:

(SEQ ID NO: 6, PiDes5) atgatggctgtaacagagggcgctgggggtgtaacggccgaggttggttt gcacaaacgcagttctcagccgcgtcccgcagctccccgcagcaagctgt tcacgttggatgaggttgcaaagcacgacagcccgactgactgctgggtg gtcattcggcggagggtttacgacgtgacgcgtgggtgccgcagcatcct ggcggaaacctgatctttgtgaaagctggccgcgactgtacccagctgtt cgattcctaccaccccttaagtgccagggctgtgctagacaagttctaca tcggtgaagtcgatgtaaggcctggggacgagcagttccttgtggctttc gaagaggacacagaggagggtcagttctacacggtcctcaagaagcgtgt ggagaagtacttcagggagaacaagctcaacccgcggcaacaggcgccat gtacgccaagtcgctgaccatcctggcgggcctggcgttgagcttctatg gtacgttctttgccttcagcagcgcaccggcctcgctgctcagcgctgtg ctgctcggcatttgcatggcggaggtgggcgtgtccatcatgcacgatgc caaccacggcgcatttgcccgcaacacgtgggcctcgcatgccctgggcg ccacgctggacatcgtgggggcatcctccttcatgtggcgccagcagcat gtcgtgggccaccatgcatacaccaacgtggacggtcaggacccagacct gcgagttaaggaccccgacgttcgccgcgtgaccaagttccagccccagc agtcgtaccaggcgtaccagcacatctacctggccttcctgtacggcctg ctggccatcaagagcgtgctgctggacgactttatggccctcagctccgg cgccatcggctccgtgaaagtggccaagctgacgcccggcgagaagctcg tgttctggggcggcaaggcgctctggctcggctactttgtgctgctgccg gtggtgaagagccgccactcctggccgctgctggcggcctgctggctgct gagcgagtttgtcacgggctggatgctggccttcatgttccaggtggcgc acgtgaccagcgatgtgagctacctggaggctgacaagacaggcaaggtc ccgaggggctgggctgccgcacaggccgccaccaccgccgactttgcgca tggctcctggttctggacccaaatttctggcggccttaactaccaggtgg tgcaccatctgttcccgggcatctgccatctgcactacccggccatcgcc ccatcgtgctggacacctgcaaggagtttaacgtgccctaccatgtgtac cccacgtttgtcagggcactcgccgcacacttcaagcatctcaaggacat gggcgccccaactgccatcccttcgctggccaccgtgggatag. In another embodiment, SEQ ID NO: 6 encodes the amino acid sequence of SEQ ID NO: 3.

In another embodiment, the isolated polynucleotide comprises a DNA sequence that is at least 60% homologous to the nucleic acid sequence of SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6, or SEQ ID NO: 8. In another embodiment, the isolated polynucleotide comprises a DNA sequence that is at least 70% homologous to the nucleic acid sequence of SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6, or SEQ ID NO: 8. In another embodiment, the isolated polynucleotide comprises a DNA sequence that is at least 75% homologous to the nucleic acid sequence of SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6, or SEQ ID NO: 8. In another embodiment, the isolated polynucleotide comprises a DNA sequence that is at least 80% homologous to the nucleic acid sequence of SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6, or SEQ ID NO: 8. In another embodiment, the isolated polynucleotide comprises a DNA sequence that is at least 85% homologous to the nucleic acid sequence of SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6, or SEQ ID NO: 8. In another embodiment, the isolated polynucleotide comprises a DNA sequence that is at least 90% homologous to the nucleic acid sequence of SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6, or SEQ ID NO: 8. In another embodiment, the isolated polynucleotide comprises a DNA sequence that is at least 95% homologous to the nucleic acid sequence of SEQ ID NO: 4, SEQ ID NO:. 5, SEQ ID NO: 6, or SEQ ID NO: 8. In another embodiment, the isolated polynucleotide comprises a DNA sequence that is at least 98% homologous to the nucleic acid sequence of SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6, or SEQ ID NO: 8.

In another embodiment, the isolated polynucleotide comprises a DNA sequence that is at least 60% identical to the nucleic acid sequence of SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6, or SEQ ID NO: 8. In another embodiment, the isolated polynucleotide comprises a DNA sequence that is at least 70% identical to the nucleic acid sequence of SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6, or SEQ ID NO: 8. In another embodiment, the isolated polynucleotide comprises a DNA sequence that is at least 75% identical to the nucleic acid sequence of SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6, or SEQ ID NO: 8. In another embodiment, the isolated polynucleotide comprises a DNA sequence that is at least 80% identical to the nucleic acid sequence of SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6, or SEQ ID NO: 8. In another embodiment, the isolated polynucleotide comprises a DNA sequence that is at least 85% identical to the nucleic acid sequence of SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6, or SEQ ID NO: 8. In another embodiment, the isolated polynucleotide comprises a DNA sequence that is at least 90% identical to the nucleic acid sequence of SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6, or SEQ ID NO: 8. In another embodiment, the isolated polynucleotide comprises a DNA sequence that is at least 95% identical to the nucleic acid sequence of SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6, or SEQ ID NO: 8. In another embodiment, the isolated polynucleotide comprises a DNA sequence that is at least 98% identical to the nucleic acid sequence of SEQ ID NO: 4, SEQ ID NO: 5, SEQ NO: 6, or SEQ ID NO: 8.

In another embodiment, the present invention comprises a desaturase or a nucleic acid molecule encoding the same combined with additional proteins and/or enzymes and/or substrates that are involved in the biosynthesis of VLC-PUFA. In another embodiment, the present invention comprises a composition comprising a desaturase or a nucleic acid molecule encoding the same combined with additional proteins and/or enzymes and/or substrates that are involved in the biosynthesis of VLC-PUFA. In another embodiment, the present invention comprises a transgenic plant comprising a desaturase or a nucleic acid molecule encoding the same combined with additional proteins and/or enzymes and/or substrates that are involved in the biosynthesis of VLC-PUFA. In another embodiment, the present invention comprises a transgenic alga comprising a desaturase or a nucleic acid molecule encoding the same combined with additional proteins and/or enzymes and/or substrates that are involved in the biosynthesis of VLC-PUFA. In another embodiment, the present invention comprises a transfected or a transformed cell comprising a desaturase or a nucleic acid molecule encoding the same combined with additional proteins and/or enzymes and/or substrates that are involved in the biosynthesis of VLC-PUFA.

In another embodiment, the present invention comprises a desaturase or a nucleic acid molecule encoding the same combined with additional proteins and/or enzymes and/or substrates that are involved in the biosynthesis of VLC-PUFA. In another embodiment, the present invention comprises an algal desaturase or a nucleic acid molecule encoding the same combined with additional algal proteins and/or enzymes and/or substrates that are involved in the biosynthesis of VLC-PUFA. In another embodiment, the present invention provides that the alga is a microalga. In another embodiment, the present invention comprises a microalgae desaturase or a nucleic acid molecule encoding the same combined with additional microalgae proteins and/or enzymes and/or substrates that are involved in the biosynthesis of VLC-PUFA.

In another embodiment, the present invention provides that algae proteins comprise an elongase. In another embodiment an elongase is described in PCT/IL2009/001117 which is hereby incorporated in its entirety by reference. In another embodiment, the present invention provides that microalgae proteins comprise the P. incisa PiELO1 gene product. In another embodiment, the present invention provides that elongase as described herein comprises the amino acid sequence:

(SEQ ID NO: 7) MALTAAWHKYDAIVSRFVFDGLRRVGLQEIQGHPSVITAHLPFIASPTPQ VTFVLAYLLIVVCGVAALRTRKSSAPREDPAWLRLLVQAHNLVLISLSAY MSSAACYYAWKYGYRFWGTNYSPKERDMGGLIYTFYVSKLYEFVDTLIML LKGKVEQVSFLHVYHHASISTIWWAIAYVAPGGDAWYCCFLNSLVHVLMY TYYLLATLLGKDAKARRKYLWWGRYLTQFQMFQFVTMMLEAAYTWAYSPY PKFLSKLLFFYMITLLALFANFYAQKHGSSRAAKQKLQ.

In another embodiment, the elongase as described herein id encoded by a polynucleotide comprising a DNA sequence comprising the sequence:

(SEQ ID NO: 8) atggcattgacggcggcctggcacaagtacgacgctatcgttagtcgctt tgttttcgatggcttgcgcagggttggcctgcaagagattcaaggccacc cctcggtgatcaccgcccaccttcccttcatagcctccccaacgccacaa gtgacgttcgtgctggcctatctgctgattgttgtctgcggggttgccgc tctgcgtacgagaaagtcgtccgcacctcgcgaggatccggcgtggctgc gactgcttgtgcaagcgcacaacttggtgctaatcagccttagcgcctac atgtcctctgccgcctgctactatgcttggaaatacggctataggttttg gggcacaaactatagccccaaggagcgggacatgggagggctcatctata ccttttacgtgtccaagctgtacgagtttgtggatacgctgatcatgctg ctcaagggcaaggtggagcaggtttcttttttgcacgtctaccaccacgc ttccatatccacgatctggtgggcaatcgcatacgtcgcacctggtggtg acgcctggtactgctgcttcctgaactcgctggtccacgtactcatgtac acatactacctgcttgcgacgctgctgggaaaggacgccaaggcgcggcg caagtatttgtggtggggacgctacctcactcagttccagatgttccagt ttgtgacgatgatgctcgaggcagcgtacacttgggcctactctccctac cccaagtttttatcaaagctgctgttatttaCatgatcactctgttggcc ctgtttgcaaacttctatgcacagaagcatggcagcagccgggcagccaa gcaaaagctgcagtaa.

In another embodiment, the present invention provides a composition comprising a desaturase as described herein. In another embodiment, the present invention provides a composition comprising the desaturase as described herein and a VLC-PUFA elongase. In another embodiment, the present invention provides a composition comprising a protein as described herein. In another embodiment, the present invention provides a composition comprising the polynucleotide as described herein. In another embodiment, the present invention provides a composition comprising a polynucleotide encoding an elongase and the polynucleotide as described herein. In another embodiment, the present invention provides a composition comprising a vector comprising the polynucleotide as described herein. In another embodiment, the present invention provides a composition comprising a vector comprising a polynucleotide encoding an elongase and a polynucleotide as described herein. In another embodiment, the present invention provides a composition comprising a combination of vectors which comprise polynucleotides encoding an elongase and polynucleotides encoding desaturases. In another embodiment, a composition such as described herein comprises a carrier. In another embodiment, a carrier stabilizes a protein or a nucleic acid molecule of the invention. In another embodiment, one of skill in the art will readily identify a known suitable carrier to be used with the composition as described herein. In another embodiment, a carrier is a buffer such as but not limited to a phosphate buffer.

In another embodiment, one of skill in the art is able to prepare a composition comprising a desaturase as described herein. In another embodiment, one of skill in the art is able to prepare a composition comprising a combination of elongases and desaturases as described herein. In another embodiment, one of skill in the art is able to prepare a composition comprising a polynucleotide as described herein. In another embodiment, one of skill in the art is able to prepare a composition comprising a combination of polynucleotides, plasmids, vectors etc. as described herein. In another embodiment, the present invention provides a composition comprising the protein as described herein to be used in foodstuffs, dietary supplements or pharmaceutical compositions. In another embodiment, the present invention provides a composition comprising the protein as described herein to be used in industrial applications for the manufacturing of VLC-PUFAs. In another embodiment, the present invention provides a composition comprising the VLC-PUFAs, the products of the enzymes of the present invention. In another embodiment, a composition comprising VLC-PUFAs is used in foodstuffs, dietary supplements or pharmaceutical compositions.

In another embodiment, the invention includes a combination of Δ5, Δ6, and/or Δ12 desaturases. In another embodiment, the invention includes a composition comprising the combination of Δ5, Δ6, and/or Δ12 desaturases. In another embodiment, the invention includes a composition comprising the combination of Δ5, Δ6, and/or Δ12 desaturases and either ω3 or ω6 C18 substrates. In another embodiment, the invention provides that a composition comprising the combination of Δ5, Δ6, and/or Δ12 desaturases and either ω3 or ω6 C18 substrates yields DGLA, ARA, DHA and/or EPA.

In another embodiment, the invention provides conjunction of P. incisa Δ12, Δ6, and Δ5 desaturases, which are set of P. incisa genes involved in the biosynthesis of ARA. In another embodiment, the invention provides conjunction of P. incisa Δ12, Δ6, and Δ5 desaturase and Δ6 specific PUFA elongase (as described herein), which are set of P. incisa genes involved in the biosynthesis of DGLA, ARA, DHA, EPA, or any combination thereof.

In another embodiment, a desaturase as described herein comprises three histidine rich motifs (his-boxes). In another embodiment, Δ6 (PiDes6) and Δ5 (PiDes5) desaturases comprise fused cytochrome b5 at their N-terminus, supporting their microsomal localization. In another embodiment, Δ6 (PiDes6) and Δ5 (PiDes5) desaturases comprise a HPGG quartet along with four amino acids conserved in all cytochrome b5 fusion desaturases (FIG. 1).

In another embodiment, transforming a plant with an algal-derived gene such as described herein produces better results in comparison to fungal genes. In another embodiment, transforming a plant with an algal-derived gene such as described herein in combination with additional genes that encode proteins that are involved in the biosynthesis of VLC-PUFA produces better results in comparison to fungal or wild-type genes. In another embodiment, transforming a plant with an algal-derived gene such as described herein (desaturase) in combination with an elongase as described herein produces better results in comparison to fungal or wild-type genes. In another embodiment, transforming a plant with a combination of algal-derived genes such as described herein produces better results (such as ARA production) in comparison to fungal or wild-type genes. In another embodiment, transforming a plant with a combination of algal-derived desaturase genes such as described herein produces better results (such as ARA production) in comparison to fungal or wild-type genes. In another embodiment, P. incisa is the richest plant source of ARA. In another embodiment, P. incisa is the richest algal source of ARA. In another embodiment, algal-derived genes such as described herein are more effective alone or in combination than those of other sources.

In another embodiment, algae as described herein are eukaryotic organisms. In another embodiment, algae as described herein are photoautotrophic. In another embodiment, algae as described herein are mixotrophic. In another embodiment, algae as described herein are unicellular. In another embodiment, algae as described herein are multicellular. In another embodiment, algae as described herein are Excavata algae. In another embodiment, algae as described herein are Rhizaria algae. In another embodiment, algae as described herein are Chromista algae. In another embodiment, algae as described herein are Alveolata algae.

In another embodiment, an algal gene and protein of the present invention is superior when compared to its homologues with respect to efficient production of PUFAs. In another embodiment, transforming a first alga with an algal gene derived from a second alga such as described herein produces better results in comparison to fungal genes. In another embodiment, a second algal gene is a gene as described herein. In another embodiment, a first and a second algal are of different species. In another embodiment, transforming a first alga with an algal gene derived from a second alga such as described herein in combination with additional genes that encode proteins that are involved in the biosynthesis of VLC-PUFA produces better results in comparison to fungal or wild-type genes. In another embodiment, transforming an alga with an algal gene (such as desaturase) derived from a second alga such as described herein in combination with an elongase as described herein produces better results in comparison to fungal or wild-type genes. In another embodiment, transforming a first alga with a combination of algal genes derived from a second alga, a third alga, etc., such as described herein produces better results (such as ARA production) in comparison to fungal or wild-type genes. In another embodiment, transforming a first alga with a combination of algal desaturase genes derived from a second alga such as described herein produces better results (such as ARA production) in comparison to fungal or wild-type genes. In another embodiment, P. incisa is the second alga. In another embodiment, P. incisa is the source of choice for genes that are involved in the biosynthesis of VLC-PUFA. In another embodiment, P. incisa is the source of choice for genes that are involved in the biosynthesis of ARA, DHA, EPA, DGLA, or any combination thereof. In another embodiment, P. incisa-derived genes such as described herein are more effective alone or in combination than those of other sources.

In another embodiment, a DNA sequence as described herein such as but not limited to SEQ ID NO: 4-6 is used to engineer a transgenic organism. In another embodiment, DNA sequences as described herein such as but not limited to SEQ ID NO: 4-6 are used to engineer a transgenic organism or transform a cell. In another embodiment, DNA sequences as described herein such as but not limited to SEQ ID NO: 4-6 and 8 are used to engineer a transgenic organism or transform a cell. In another embodiment, the DNA sequences comprise the sequences provided in SEQ ID NO: 4-6 and 8 or variants of these sequences due, for example: base substitutions, deletions, and/or additions.

In another embodiment, the present invention provides transgenic plant oils enriched with VLC-PUFA. In another embodiment, the present invention provides transgenic alga oils enriched with VLC-PUFA. In another embodiment, the present invention provides the reconstitution of C20-VLC-PUFA biosynthesis in oil-synthesizing seeds of higher plants. In another embodiment, the present invention provides expanded use by enhancement of the levels of ARA, DGLA, DHA, EPA, or a combination thereof in the transgenic plants.

In another embodiment, the present invention provides an expression vector comprising the polynucleotide as described herein. In another embodiment, the present invention provides a combination of expression vectors each comprising a polynucleotide as described herein. In another embodiment, the present invention provides an expression vector comprising a combination of polynucleotides as described herein. In another embodiment, the present invention provides a plant specific expression vector comprising the polynucleotide or combination of polynucleotides as described herein. In another embodiment, the present invention provides an algal specific expression vector comprising the polynucleotide or combination of polynucleotides as described herein. In another embodiment, the present invention provides a cell comprising the expression vector/s as described herein. In another embodiment, the expression vector/s is contained within an agrobacterium. In another embodiment, a cell is a plant cell or an algal cell. In another embodiment, a plant is an oil crop. In another embodiment, the transformed plant is an oil crop.

In another embodiment, the present invention provides a transgenic plant, a transgenic seed, or a transgenic alga transformed by a polynucleotide as described herein. In another embodiment, the present invention provides a transgenic plant, a transgenic seed, or a transgenic alga transformed by any combination of polynucleotides as described herein. In another embodiment, the present invention provides that the transgenic plant is a true-breeding for the polynucleotide/s as described herein. In another embodiment, the present invention provides a transgenic seed, produced by a transgenic plant transformed by the polynucleotide/s as described herein. In another embodiment, a transgenic plant, a transgenic seed, or a transgenic alga as described herein produces very long-chain polyunsaturated fatty acid (VLC-PUFA). In another embodiment, a transgenic plant, a transgenic seed, or a transgenic alga as described herein produces arachidonic acid. In another embodiment, a transgenic plant or a transgenic seed as described herein produces DHA. In another embodiment, a transgenic plant, a transgenic seed, or a transgenic alga as described herein produces DGLA.

In another embodiment, the present invention provides a method of producing very long-chain polyunsaturated fatty acid (VLC-PUFA) in a plant, a plant cell, or an alga comprising the step of transforming a plant, a plant cell, or an alga with a polynucleotide as described herein. In another embodiment, the present invention unexpectedly provides an utmost efficient method of producing very long-chain polyunsaturated fatty acid (VLC-PUFA) in a plant, a plant cell, or an alga comprising the step of transforming a plant, a plant cell, or an alga with a polynucleotide as described herein. In another embodiment, a VLC-PUFA is produced from γ-linolenic acid (GLA).

In another embodiment, a VLC-PUFA is produced from stearidonic acid (SDA). In another embodiment, a VLC-PUFA is produced from GLA, SDA, or their combination. In another embodiment, a VLC-PUFA comprises 20 carbons. In another embodiment, a VLC-PUFA is 20:3ω6 or 20:4ω3. In another embodiment, a VLC-PUFA is produced by the protein/s as described herein in a cell or a plant, a plant cell, or an alga. In another embodiment, a VLC-PUFA is produced by the protein/s as described herein in a cell, a plant, a plant cell, or an alga under oleogenic conditions. In another embodiment, an unexpected amount of VLC-PUFA is produced by the protein/s as described herein in a cell, an alga, or a plant under nitrogen starvation conditions.

In another embodiment, a cell is a eukaryotic cell. In another embodiment, a cell is a prokaryotic cell. In another embodiment, a cell is a plant cell. In another embodiment, a cell is an algal cell. In another embodiment, a cell is a transfected cell. In another embodiment, a cell is transiently transfected with a polynucleotide or a combination of polynucleotides as described herein. In another embodiment, a cell is stably transfected with a polynucleotide or a combination of polynucleotides as described herein. In another embodiment, the present invention provides a method of enhancing oil storage, EPA accumulation, DHA accumulation, ARA accumulation, DGLA accumulation, or a combination thereof in a cell, comprising the step of transforming a cell with a polynucleotide as described herein. In another embodiment, the present invention provides a method of enhancing oil storage, EPA accumulation, DHA accumulation, ARA accumulation, DGLA accumulation, or a combination thereof in a cell, comprising the step of transfecting a cell with a polynucleotide as described herein. In another embodiment, the present invention provides a method of enhancing oil storage, EPA accumulation, DHA accumulation, DGLA accumulation, ARA accumulation, or a combination thereof in a cell, comprising the step of transforming a cell with a combination of polynucleotides as described herein. In another embodiment, the present invention provides a method of enhancing oil storage, EPA accumulation, DHA accumulation, ARA accumulation, DGLA accumulation, or a combination thereof in a cell or a multicellular organism, comprising the step of transforming a cell or a multicellular organism with a polynucleotide as described herein. In another embodiment, the present invention provides a method of enhancing oil storage, EPA accumulation, DGLA accumulation, DHA accumulation, ARA accumulation, or a combination thereof in a multicellular organism, comprising the step of transforming a multicellular organism with a combination of polynucleotides as described herein. In another embodiment, the multicellular organism or cell is grown under nitrogen starvation conditions, oleogenic conditions, or a combination thereof.

In another embodiment, transformation as used herein comprises “transduction”. In another embodiment, transformation as used herein comprises transfection. In another embodiment, transformation as used herein comprises “conjugation”. In another embodiment, transformation as used herein applies to eukaryotic and prokaryotic cells. In another embodiment, transformation as used herein comprises the insertion of new genetic material into nonbacterial cells including animal and plant cells.

In another embodiment, the present invention provides a method of enhancing oil storage, EPA accumulation, DHA accumulation, DGLA accumulation, ARA accumulation, or a combination thereof in a plant cell, comprising the step of transforming a plant cell with a polynucleotide as described herein. In another embodiment, the present invention provides a method of enhancing oil storage, EPA accumulation, DHA accumulation, ARA accumulation, DGLA accumulation, or a combination thereof in a plant cell, comprising the step of transforming a plant cell with a combination of polynucleotides as described herein. In another embodiment, the present invention provides a method of enhancing oil storage, EPA accumulation, DHA accumulation, ARA accumulation, DGLA accumulation, or a combination thereof in a plant, comprising the step of transforming a plant with a polynucleotide as described herein. In another embodiment, the present invention provides a method of enhancing oil storage, EPA accumulation, DHA accumulation, ARA accumulation, DGLA accumulation, or a combination thereof in a plant, comprising the step of transforming a plant with a combination of polynucleotides as described herein. In another embodiment, the plant or plant cell is grown under nitrogen starvation conditions, oleogenic conditions, or a combination thereof.

In another embodiment, the invention further provides an engineered organism, such as a transgenic plant. In another embodiment, the invention further provides an engineered organism, such as a transgenic seed. In another embodiment, the invention further provides an engineered organism, such as a transgenic alga. In another embodiment, the invention further provides an engineered organism, such as a transgenic animal. In another embodiment, an engineered organism is engineered to express a protein as described herein. In another embodiment, an engineered organism is engineered to express a combination of proteins as described herein. In another embodiment, an engineered organism is engineered to express elevated levels of the protein or a combination of proteins. In another embodiment, an engineered plant as described herein is used for manufacturing desired PUFAs such as but not limited to ARA. In another embodiment, an engineered plant as described herein is used for manufacturing desired PUFAs such as ARA at a reduced cost.

In another embodiment, an engineered organism comprises a synthetic pathway for the production of a protein. In another embodiment, an engineered organism comprising a synthetic pathway for the production of the protein allows greater control over the production of PUFAs by the pathway by an organism. In another embodiment, the pathway includes but is not limited to A′-fatty acid desaturase, and/or A′-fatty acid desaturase.

In another embodiment, an engineered cell, plant or seed comprises an oligonucleotide as described herein. In another embodiment, an engineered plant or seed produces a protein as described herein and comprises an oligonucleotide as described herein. In another embodiment, an engineered plant or seed produces proteins as described herein and comprises oligonucleotides as described herein.

In another embodiment, the invention provides a method of producing very long-chain polyunsaturated fatty acid (VLC-PUFA) in a cell, a plant, a plant cell, or an alga, comprising the step of transforming a plant, a plant cell, or an alga with a polynucleotide as described herein, thereby producing a VLC-PUFA in a plant, a plant cell, or an alga. In another embodiment, the invention provides a method of producing very long-chain polyunsaturated fatty acid (VLC-PUFA) in a cell, a plant, a plant cell, or an alga, comprising the step of transforming a plant, a plant cell, or an alga with an exogenous polynucleotide as described herein, thereby producing a VLC-PUFA in a cell, a plant, a plant cell, or an alga. In another embodiment, the invention provides a method of producing very long-chain polyunsaturated fatty acid (VLC-PUFA) in a cell, a plant, a plant cell, or an alga, comprising the step of transforming a plant, a plant cell, or an alga with a vector comprising an exogenous polynucleotide as described herein, thereby producing a VLC-PUFA in a cell; a plant, a plant cell, or an alga. In another embodiment, the invention provides a method of producing very long-chain polyunsaturated fatty acid (VLC-PUFA) in a cell, a plant, a plant cell, or an alga, comprising the step of transforming a plant, a plant cell, or an alga with a combination of vectors comprising a combination of exogenous polynucleotides as described herein, thereby producing a VLC-PUFA in a cell, a plant, a plant cell, or an alga. In another embodiment, the invention provides a method of producing very long-chain polyunsaturated fatty acid (VLC-PUFA) in a cell, a plant, a plant cell, or an alga, comprising the step of transforming a cell, a plant, a plant cell, or an alga with a combination of exogenous polynucleotides as described herein, thereby producing a VLC-PUFA in a cell, a plant, a plant cell, or an alga.

In another embodiment, the invention provides that a plant, a cell, a plant cell, or an alga as described herein is treated or supplemented with linoleic acid (LA; 18:2ω6), α-linolenic acid (ALA; 18:3ω3), oleic acid (18:1), dihomo-gamma-linolenic acid (20:3ω6), phosphatidylcholine (PC), diacylglyceroltrimethylhomoserine (DGTS), phosphatidylethanolamine (PE), or any combination thereof, before transformation, after transformation, during transformation or a combination thereof.

In another embodiment, the invention provides that the VLC-PUFA is eicosapentaenoic acid (EPA, 20:5ω3). In another embodiment, the invention provides that the VLC-PUFA is docosahexaenoic acid (DHA, 22:6ω3). In another embodiment, the invention provides that the VLC-PUFA is arachidonic acid (ARA, 20:4ω6). In another embodiment, the invention provides that a cell, a plant, or an alga transformed by a polynucleotide or a combination of polynucleotides as described herein, is grown under oleogenic conditions. In another embodiment, the invention provides that a cell, a plant, or an alga transformed by a polynucleotide or a combination of polynucleotides as described herein, is grown under nitrogen starvation conditions.

In another embodiment, the invention provides that producing very long-chain polyunsaturated fatty acid (VLC-PUFA) is enhancing oil storage, arachidonic acid accumulation, eicosapentaenoic acid accumulation, docosahexaenoic acid accumulation, or a combination thereof that a cell, a plant, or an alga transformed by a polynucleotide or a combination of polynucleotides as described herein

In another embodiment, a PUFA is di-homo-gamma-linolenic acid, arachidonic acid, eicosapentaenoic acid, docosatrienoic acid, docosatetraenoic acid, docosapentaenoic acid or docosahexaenoic acid. In another embodiment, a PUFA is a 24 carbon fatty acid with at least 4 double bonds.

In another embodiment, expression of the protein/s of the invention in plants or seed requires subcloning an ORF/s sequence encoding the protein/s into a plant expression vector, which may comprise a viral 35S promoter, and a Nos terminator. In another embodiment, a cassette or promoter/coding sequence/terminator is then be subcloned into the plant binary transformation vector, and the resulting plasmid introduced into Agrobacterium. In another embodiment, the Agrobacterium strain transforms the plant. In another embodiment, the. Agrobacterium strain transforms the plant by the vacuum-infiltration of inflorescences, and the seeds harvested and plated onto selective media containing an antibiotic. In another embodiment, the plasmid confers resistance to an antibiotic, thus only transformed plant material will grow in the presence of an antibiotic. In another embodiment, resistant lines are identified and self-fertilized to produce homozygous material. In another embodiment, leaf material is analyzed for expression of the protein comprising desaturase activity. In another embodiment, leaf material is analyzed for expression of a combination of protein comprising desaturase and elongase activities.

In some embodiments, the terms “protein”, “desaturase”, or “polypeptide” are used interchangeably. In some embodiments, “protein”, “desaturase”, or “polypeptide” as used herein encompasses native polypeptides (either degradation products, synthetically synthesized polypeptides or recombinant polypeptides) and peptidomimetics (typically, synthetically synthesized polypeptides), as well as peptoids and semipeptoids which are polypeptide analogs, which have, in some embodiments, modifications rendering the polypeptides/proteins even more stable while in a body or more capable of penetrating into cells.

In some embodiments, modifications include, but are not limited to N terminus modification, C terminus modification, polypeptide bond modification, including, but not limited to, CH2—NH, CH2—S, CH2—S═O, O═C—NH, CH2—O, CH2—CH2, S═C—NH, CH═CH or CF═CH, backbone modifications, and residue modification. Methods for preparing peptidomimetic compounds are well known in the art and are specified, for example, in Quantitative Drug Design, C. A. Ramsden Gd., Chapter 17.2, F. Choplin Pergamon Press (1992), which is incorporated by reference as if fully set forth herein. Further details in this respect are provided hereinunder.

In some embodiments, polypeptide bonds (—CO—NH—) within the polypeptide are substituted. In some embodiments, the polypeptide bonds are substituted by N-methylated bonds (—N(CH3)—CO—). In some embodiments, the polypeptide bonds are substituted by ester bonds (—C(R)H—C—O—O—C(R)—N—). In some embodiments, the polypeptide bonds are substituted by ketomethylene bonds (—CO—CH2—). In some embodiments, the polypeptide bonds are substituted by α-aza bonds (—NH—N(R)—CO—), wherein R is any alkyl, e.g., methyl, carbo bonds (—CH2—NH—). In some embodiments, the polypeptide bonds are substituted by hydroxyethylene bonds (—CH(OH)—CH2—). In some embodiments, the polypeptide bonds are substituted by thioamide bonds (—CS—NH—). In some embodiments, the polypeptide bonds are substituted by olefmic double bonds (—CH=CH—). In some embodiments, the polypeptide bonds are substituted by retro amide bonds (—NH—CO—). In some embodiments, the polypeptide bonds are substituted by polypeptide derivatives (—N(R)—CH2—CO—), wherein R is the “normal” side chain, naturally presented on the carbon atom. In some embodiments, these modifications occur at any of the bonds along the polypeptide chain and even at several (2-3 bonds) at the same time.

In some embodiments, natural aromatic amino acids of the polypeptide such as Trp, Tyr and Phe, be substituted for synthetic non-natural acid such as Phenylglycine, TIC, naphthylelanine (Nol), ring-methylated derivatives of Phe, halogenated derivatives of Phe or o-methyl-Tyr. In some embodiments, the polypeptides of the present invention include one or more modified amino acid or one or more non-amino acid monomers (e.g., fatty acid, complex carbohydrates, etc.).

In one embodiment, “amino acid” or “amino acids” is understood to include the 20 naturally occurring amino acid; those amino acid often modified post-translationally in vivo, including, for example, hydroxyproline, phosphoserine and phosphothreonine; and other unusual amino acid including, but not limited to, 2-aminoadipic acid, hydroxylysine, isodesmosine, nor-valine, nor-leucine and ornithine. In one embodiment, “amino acid” includes both D- and L-amino acid.

In some embodiments, the polypeptides or proteins of the present invention are utilized in a soluble form. In some embodiments, the polypeptides or proteins of the present invention include one or more non-natural or natural polar amino acid, including but not limited to serine and threonine which are capable of increasing polypeptide or protein solubility due to their hydroxyl-containing side chain.

In some embodiments, the polypeptides or proteins of the present invention are utilized in a linear form, although it will be appreciated by one skilled in the art that in cases where cyclization does not severely interfere with polypeptide characteristics, cyclic forms of the polypeptide can also be utilized.

In some embodiments, the polypeptides or proteins of present invention are biochemically synthesized such as by using standard solid phase techniques. In some embodiments, these biochemical methods include exclusive solid phase synthesis, partial solid phase synthesis, fragment condensation, or classical solution synthesis. In some embodiments, these methods are used when the polypeptide is relatively short (about 5-15 kDa) and/or when it cannot be produced by recombinant techniques (i.e., not encoded by a nucleic acid sequence) and therefore involves different chemistry.

In some embodiments, solid phase polypeptide or protein synthesis procedures are well known to one skilled in the art and further described by John Morrow Stewart and Janis Dillaha Young, Solid Phase Polypeptide Syntheses (2nd Ed., Pierce Chemical Company, 1984). In some embodiments, synthetic polypeptides or proteins are purified by preparative high performance liquid chromatography [Creighton T. (1983) Proteins, structures and molecular principles. WH Freeman and Co. N.Y.], and the composition of which can be confirmed via amino acid sequencing by methods known to one skilled in the art.

In some embodiments, recombinant protein techniques are used to generate the polypeptides of the present invention. In some embodiments, recombinant protein techniques are used for generation of relatively long polypeptides (e.g., longer than 18-25 amino acid). In some embodiments, recombinant protein techniques are used for the generation of large amounts of the polypeptide of the present invention. In some embodiments, recombinant techniques are described by Bitter et al., (1987) Methods in Enzymol. 153:516-544, Studier et al. (1990) Methods in Enzymol. 185:60-89, Brisson et al. (1984) Nature 310:511-514, Takamatsu et al. (1987) EMBO J. 6:307-311, Coruzzi et al. (1984) EMBO J. 3:1671-1680 and Brogli et al, (1984) Science 224:838-843, Gurley et al. (1986) Mol. Cell. Biol. 6:559-565 and Weissbach & Weissbach, 1988, Methods for Plant Molecular Biology, Academic Press, NY, Section VIII, pp 421-463.

In one embodiment, a polypeptide or protein of the present invention is synthesized using a polynucleotide encoding a polypeptide or protein of the present invention. In some embodiments, the polynucleotide encoding a polypeptide of the present invention is ligated into an expression vector, comprising a transcriptional control of a cis-regulatory sequence (e.g., promoter sequence). In some embodiments, the cis-regulatory sequence is suitable for directing constitutive expression of the polypeptide of the present invention. In some embodiments, the cis-regulatory sequence is suitable for directing tissue specific expression of the polypeptide of the present invention. In some embodiments, the cis-regulatory sequence is suitable for directing inducible expression of the polypeptide of the present invention. In another embodiment, a polypeptide is a protein comprising a desaturase as described herein.

In another embodiment, the polynucleotide comprises a genomic polynucleotide sequence. In another embodiment, the polynucleotide comprises a composite polynucleotide sequence.

In one embodiment, the phrase “a polynucleotide” refers to a single or double stranded nucleic acid sequence which be isolated and provided in the form of an RNA sequence, a complementary polynucleotide sequence (cDNA), a genomic polynucleotide sequence and/or a composite polynucleotide sequences (e.g., a combination of the above).

In one embodiment, “genomic polynucleotide sequence” refers to a sequence derived (isolated) from a chromosome and thus it represents a contiguous portion of a chromosome.

In one embodiment, “composite polynucleotide sequence” refers to a sequence, which is at least partially complementary and at least partially genomic. In one embodiment, a composite sequence can include some exonal sequences required to encode the polypeptide of the present invention, as well as some intronic sequences interposing there between. In one embodiment, the intronic sequences can be of any source, including of other genes, and typically will include conserved splicing signal sequences. In one embodiment, intronic sequences include cis acting expression regulatory elements.

In one embodiment, the polynucleotides of the present invention further comprise a signal sequence encoding a signal peptide for the secretion of the polypeptides of the present invention. In one embodiment, following expression, the signal peptides are cleaved from the precursor proteins resulting in the mature proteins.

In some embodiments, polynucleotides of the present invention are prepared using PCR techniques or any other method or procedure known to one skilled in the art. In some embodiments, the procedure involves the legation of two different DNA sequences (See, for example, “Current Protocols in Molecular Biology”, eds. Ausubel et al., John Wiley & Sons, 1992).

In one embodiment, polynucleotides of the present invention are inserted into expression vectors (i.e., a nucleic acid construct) to enable expression of the recombinant polypeptide. In one embodiment, the expression vector of the present invention includes additional sequences which render this vector suitable for replication and integration in prokaryotes. In one embodiment, the expression vector of the present invention includes additional sequences which render this vector suitable for replication and integration in eukaryotes. In one embodiment, the expression vector of the present invention includes a shuttle vector which renders this vector suitable for replication and integration in both prokaryotes and eukaryotes. In some embodiments, cloning vectors comprise transcription and translation initiation sequences (e.g., promoters, enhancers) and transcription and translation terminators (e.g., polyadenylation signals).

In one embodiment, a variety of prokaryotic or eukaryotic cells can be used as host-expression systems to express the polypeptides of the present invention. In some embodiments, these include, but are not limited to, microorganisms, such as bacteria transformed with a recombinant bacteriophage DNA, plasmid DNA or cosmid DNA expression vector containing the polypeptide coding sequence; yeast transformed with recombinant yeast expression vectors containing the polypeptide coding sequence; plant cell systems infected with recombinant virus expression vectors (e.g., cauliflower mosaic virus, CaMV; tobacco mosaic virus, TMV) or transformed with recombinant plasmid expression vectors, such as Ti plasmid, containing the polypeptide coding sequence.

In some embodiments, non-bacterial expression systems are used (e.g., plant expression systems) to express the polypeptide of the present invention.

In one embodiment, yeast expression systems are used. In one embodiment, algae expression systems are used. In one embodiment, plant expression systems are used. In one embodiment, a number of vectors containing constitutive or inducible promoters can be used in yeast as disclosed in U.S. Pat. No. 5,932,447 which is hereby incorporated in its entirety by reference. In another embodiment, vectors which promote integration of foreign DNA sequences into the yeast chromosome are used.

In another embodiment, expression in a host cell can be accomplished in a transient or a stable fashion. In another embodiment, a host cell is a cell as described herein. In another embodiment, transient expression is from introduced constructs which contain expression signals functional in the host cell, but which constructs do not replicate and rarely integrate in the host cell, or where the host cell is not proliferating. In another embodiment, transient expression also can be accomplished by inducing the activity of a regulatable promoter operably linked to the gene of interest.

In another embodiment, stable expression is achieved by introduction of a construct that integrates into the host genome. In another embodiment, stable expression comprises autonomously replication within the host cell. In another embodiment, stable expression of the polynucleotide of the invention is selected for through the use of a selectable marker located on or transfected with the expression construct, followed by selection for cells expressing the marker. In another embodiment, stable expression results from integration, the site of the construct's integration can occur randomly within the host genome or can be targeted through the use constructs containing regions of homology with the host genome sufficient to target recombination with the host locus. In another embodiment, constructs are targeted to an endogenous locus, all or some of the transcriptional and translational regulatory regions can be provided by the endogenous locus.

In another embodiment, an expression of a protein as described herein comprising desaturase activity includes functional transcriptional and translational initiation and termination regions that are operably, linked to the DNA encoding the protein comprising a desaturase activity. In another embodiment, an expression of proteins as described herein comprising various desaturase activities includes functional transcriptional and translational initiation and termination regions that are operably linked to the DNA encoding the proteins comprising desaturase activity. In another embodiment, an expression of proteins as described herein comprising desaturase and elongase activities includes functional transcriptional and translational initiation and termination regions that are operably linked to the DNA encoding each protein comprising a desaturase or elongase activity. In another embodiment, transcriptional and translational initiation and termination regions are derived from a variety of nonexclusive sources, including the DNA to be expressed, genes known or suspected to be capable of expression in the desired system, expression vectors, chemical synthesis, or from an endogenous locus in a host cell. hi another embodiment, expression in a plant tissue and/or plant part presents certain efficiencies, particularly where the tissue or part is one which is harvested early, such as seed, leaves, fruits, flowers, roots, etc. In another embodiment, expression can be targeted to that location in a plant by utilizing specific regulatory sequences that are lcnown to one of skill in the art. In another embodiment, the expressed protein is an enzyme which produces a product which may be incorporated, either directly or upon further modifications, into a fluid fraction from the host plant. In another embodiment, expression of a protein of the invention, or antisense thereof, alters the levels of specific PUFAs, or derivatives thereof, found in plant parts and/or plant tissues. The desaturase coding region, in some embodiments, may be expressed either by itself or with other genes such as but not limited to elongase, in order to produce cells, tissues, algae, and/or plant parts containing higher proportions of desired PUFAs or in which the PUFA composition more closely resembles that of human breast milk. In another embodiment, the termination region is derived from the 3′ region of the gene from which the initiation region was obtained or from a different gene. In another embodiment, the termination region usually is selected as a matter of convenience rather than because of any particular property.

In another embodiment, a plant or plant tissue is utilized as a host or host cell, respectively, for expression of the protein of the invention which may, in turn, be utilized in the production of polyunsaturated fatty acids. In another embodiment, desired PUFAS are expressed in seed. In another embodiment, methods of isolating seed oils are known in the art. In another embodiment, seed oil components are manipulated through the expression of the protein of the invention in order to provide seed oils that can be added to nutritional compositions, pharmaceutical compositions, animal feeds and cosmetics. In another embodiment, a vector which comprises a DNA sequence encoding the protein as described herein is linked to a promoter, and is introduced into the plant tissue or plant for a time and under conditions sufficient for expression of the protein.

In another embodiment, a vector as described herein comprises additional genes that encode other enzymes, for example, elongase, Δ4-desaturase, a different Δ5-desaturase, a different Δ6-desaturase, Δ10-desaturase, a different Δ12-desaturase, Δ15-desaturase, Δ17-desaturase, Δ19-desaturase, or any combination thereof. In another embodiment, the plant tissue or plant produces the relevant substrate upon which the enzymes act or a vector encoding enzymes which produce such substrates may be introduced into the plant tissue, plant cell or plant. In another embodiment, a substrate is sprayed on plant tissues expressing the appropriate enzymes. In another embodiment, the invention is directed to a transgenic plant comprising the above-described vector, wherein expression of the nucleotide sequence of the vector results in production of a polyunsaturated fatty acid in, for example, the seeds of the transgenic plant.

In another embodiment, the regeneration, development, and cultivation of plants from single plant protoplast transformants or from various transformed explants is well known in the art (for example: Weissbach and Weissbach, In: Methods for Plant Molecular Biology, (Eds.),

Academic Press, Inc. San Diego, Calif., (1988)). In another embodiment, regeneration and growth process comprises the steps of selection of transformed cells, culturing those individualized cells through the usual stages of embryonic development through the rooted plantlet stage. In another embodiment, transgenic embryos and seeds are similarly regenerated. In another embodiment, resulting transgenic rooted shoots are thereafter planted in an appropriate plant growth medium such as soil. In another embodiment, regeneration and growth process of algae are known to one of skill in the art. In another embodiment, identification, selection, of transgenic algae are known to one of skill in the art.

In another embodiment, development or regeneration of plants containing an exogenous polynucleotide as described herein encodes a protein as described herein and is well known in the art. In another embodiment, development or regeneration of algae containing an exogenous polynucleotide as described herein encodes a protein as described herein and is well known in the art. In another embodiment, the regenerated plants are self-pollinated to provide homozygous transgenic plants. In another embodiment, pollen obtained from the regenerated plants is crossed to seed-grown plants of agronomically important lines. In another embodiment, pollen from plants of these important lines is used to pollinate regenerated plants. In another embodiment, a transgenic plant of the present invention containing a desired polypeptide is cultivated using methods well known to one skilled in the art.

In another embodiment, a variety of methods can be utilized for the regeneration of plants from plant tissue. In another embodiment, the method of regeneration will depend on the starting plant tissue and the particular plant species to be regenerated. In another embodiment, methods for transforming dicots, primarily by use of Agrobacterium tumefaciens, and obtaining transgenic plants are known in the art McCabe et al., Biol. Technology 6:923 (1988), Christou et al., Plant Physiol. 87:671-674 (1988)); Cheng et al., Plant Cell Rep. 15:653657 (1996), McKently et al., Plant Cell Rep. 14:699-703 (1995)); Grant et al., Plant Cell Rep. 15:254-258, (1995).

In another embodiment, transformation of monocotyledons using electroporation, particle bombardment, and Agrobacterium are known. In another embodiment, transformation and plant regeneration are well established in the art. In another embodiment, assays for gene expression based on the transient expression of cloned nucleic acid constructs have been developed by introducing the nucleic acid molecules into plant cells by polyethylene glycol treatment, electroporation, or particle bombardment (Marcotte et al., Nature 335:454-457 (1988); Marcotte et al., Plant Cell 1:523-532 (1989); McCarty et al., Cell 66:895-905 (1991); Hattori et al., Genes Dev. 6:609-618 (1992); Goff et al., EMBO J. 9:2517-2522 (1990)).

In another embodiment, transient expression systems are used to functionally dissect the oligonucleotides constructs. In another embodiment, practitioners are familiar with the standard resource materials which describe specific conditions and procedures for the construction, manipulation and isolation of macromolecules (e.g., DNA molecules, plasmids, etc.), generation of recombinant organisms and the screening and isolating of clones, (see for example,: Sambrook et al., Molecular Cloning: A Laboratory Manual, Cold Spring Harbor Press (1989); Maliga et al., Methods in Plant Molecular Biology, Cold Spring Harbor Press (1995); Birren et al., Genome Analysis: Detecting Genes, 1, Cold Spring Harbor, N.Y. (1998); Birren et al., Genome Analysis: Analyzing DNA, 2, Cold Spring Harbor, N.Y. (1998); Plant Molecular Biology: A Laboratory Manual, eds. Clark, Springer, N.Y. (1997)).

In one embodiment, the expression vector of the present invention can further include additional polynucleotide sequences that allow, for example, the translation of several proteins from a single mRNA such as an internal ribosome entry site (IBES) and sequences for genomic integration of the promoter-chimeric polypeptide.

In some embodiments, expression vectors containing regulatory elements from eukaryotic viruses such as retroviruses are used by the present invention. In some embodiments, recombinant viral vectors are useful for in vivo expression of the polypeptides of the present invention since they offer advantages such as lateral infection and targeting specificity. In one embodiment, lateral infection is inherent in the life cycle of, for example, retrovirus, and is the process by which a single infected cell produces many progeny virions that bud off and infect neighboring cells. In one embodiment, the result is that a large area becomes rapidly infected, most of which was not initially infected by the original viral particles. In one embodiment, viral vectors are produced that are unable to spread laterally. In one embodiment, this characteristic can be useful if the desired purpose is to introduce a specified gene into only a localized number of targeted cells.

In one embodiment, various methods can be used to introduce the expression vector of the present invention into cells. Such methods are generally described in Sambrook et al., Molecular Cloning: A Laboratory Manual, Cold Springs Harbor Laboratory, New York (1989, 1992), in Ausubel et al., Current Protocols in Molecular Biology, John Wiley and Sons, Baltimore, Md. (1989), Chang et al., Somatic Gene Therapy, CRC Press, Ann Arbor, Mich. (1995), Vega et al., Gene Targeting, CRC Press, Ann Arbor Mich. (1995), Vectors: A Survey of Molecular Cloning Vectors and Their Uses, Butterworths, Boston Mass. (1988) and Gilboa et al. [Biotechniques 4 (6): 504-512, 1986] and include, for example, stable or transient transfection, lipofection, electroporation and infection with recombinant viral vectors. In addition, see U.S. Pat. Nos. 5,464,764 and 5,487,992 for positive-negative selection methods.

In one embodiment, plant expression vectors are used. In one embodiment, the expression of a polypeptide coding sequence is driven by a number of promoters. In some embodiments, viral promoters such as the 35S RNA and 19S RNA promoters of CaMV [Brisson et al., Nature 310:511-514 (1984)], or the coat protein promoter to TMV [Takamatsu et al., EMBO J. 6:307-311 (1987)] are used. In another embodiment, plant promoters are used such as, for example, the small subunit of RUBISCO [Coruzzi et al., EMBO J. 3:1671-1680 (1984); and Brogli et al., Science 224:838-843 (1984)] or heat shock promoters, e.g., soybean hsp17.5-E or hsp17.3-B [Gurley et al., Mol. Cell. Biol. 6:559-565 (1986)]. In one embodiment, constructs are introduced into plant cells using Ti plasmid, Ri plasmid, plant viral vectors, direct DNA transformation, microinjection, electroporation and other techniques well known to the skilled artisan. See, for example, Weissbach & Weissbach [Methods for Plant Molecular Biology, Academic Press, NY, Section VIII, pp 421-463(1988)]. Other expression systems such as insects and mammalian host cell systems, which are well known in the art, can also be used by the present invention.

It will be appreciated that other than containing the necessary elements for the transcription and translation of the inserted coding sequence (encoding the polypeptide or protein), the expression construct of the present invention can also include sequences engineered to optimize stability, production, purification, yield or activity of the expressed polypeptide or protein.

In some embodiments, transformed cells are cultured under effective conditions, which allow for the expression of high amounts of recombinant polypeptide or protein. In some embodiments, effective culture conditions include, but are not limited to, effective media, bioreactor, temperature, pH and oxygen conditions that permit protein production. In one embodiment, an effective medium refers to any medium in which a cell is cultured to produce the recombinant polypeptide or protein of the present invention. In some embodiments, a medium typically includes an aqueous solution having assimilable carbon, nitrogen and phosphate sources, and appropriate salts, minerals, metals and other nutrients, such as vitamins. In some embodiments, cells of the present invention can be cultured in conventional fermentation bioreactors, shake flasks, test tubes, microtiter dishes and petri plates. In some embodiments, culturing is carried out at a temperature, pH and oxygen content appropriate for a recombinant cell. In some embodiments, culturing conditions are within the expertise of one of ordinary skill in the art.

In some embodiments, depending on the vector and host system used for production, resultant polypeptides or proteins of the present invention either remain within the recombinant cell, secreted into the fermentation medium, secreted into a space between two cellular membranes, or retained on the outer surface of a cell or viral membrane.

In one embodiment, following a predetermined time in culture, recovery of the recombinant polypeptide or protein is effected.

In one embodiment, the phrase “recovering the recombinant polypeptide or protein” used herein refers to collecting the whole fermentation medium containing the polypeptide or protein and need not imply additional steps of separation or purification.

In one embodiment, polypeptides or proteins of the present invention are purified using a variety of standard protein purification techniques, such as, but not limited to, affinity chromatography, ion exchange chromatography, filtration, electrophoresis, hydrophobic interaction chromatography, gel filtration chromatography, reverse phase chromatography, concanavalin A chromatography, chromatofocusing and differential solubilization.

In one embodiment, to facilitate recovery, the expressed coding sequence can be engineered to encode the polypeptide or proteins of the present invention and fused cleavable moiety. In one embodiment, a fusion protein can be designed so that the polypeptide or protein can be readily isolated by affinity chromatography; e.g., by immobilization on a column specific for the cleavable moiety. In one embodiment, a cleavage site is engineered between the polypeptide or protein and the cleavable moiety and the polypeptide or protein can be released from the chromatographic column by treatment with an appropriate enzyme or agent that specifically cleaves the fusion protein at this site [e.g., see Booth et al., Immunol. Lett. 19:65-70 (1988); and Gardella et al., J. Biol. Chem. 265:15854-15859 (1990)].

In one embodiment, the polypeptide or protein of the present invention is retrieved in “substantially pure” form.

In one embodiment, the phrase “substantially pure” refers to a purity that allows for the effective use of the protein in the applications described herein.

In one embodiment, the polypeptide or protein of the present invention can also be synthesized using in vitro expression systems. In one embodiment, in vitro synthesis methods are well known in the art and the components of the system are commercially available.

In another embodiment, the invention comprises a process for making a very long-chain polyunsaturated fatty acid produced by the protein or combination of proteins of the invention in a cell as described herein. In another embodiment, the resulting very long-chain polyunsaturated fatty acid produced by the transgenic cell or organism as described herein is utilized as a food additive. In another embodiment, a very long-chain polyunsaturated fatty acid produced by the transgenic cell or organism as described herein is utilized as a supplement. In another embodiment, a very long-chain polyunsaturated fatty acid produced by the transgenic cell or organism as described herein is administered to a human subject. In another embodiment, a very long-chain polyunsaturated fatty acid produced by the transgenic cell or organism as described herein is administered to a baby. In another embodiment, a very long-chain polyunsaturated fatty acid produced by the transgenic cell or organism as described herein is administered to an infant. In another embodiment, a very long-chain polyunsaturated fatty acid produced by the transgenic cell or organism as described herein is administered to an animal. In another embodiment, a very long-chain polyunsaturated fatty acid produced by the transgenic cell or organism as described herein is administered to a mammal. In another embodiment, a very long-chain polyunsaturated fatty acid produced by the transgenic cell or organism as described herein is administered to a farm animal, a rodent, a pet, or a lab animal.

In another embodiment, the described pharmaceutical and nutritional compositions are utilized in connection with animals (i.e., domestic or non-domestic), as well as humans, as animals experience many of the same needs and conditions as humans. For example, the oil or acids of the present invention may be utilized in animal or aquaculture feed supplements, animal feed substitutes, animal vitamins or in animal topical ointments.

In another embodiment, a very long-chain polyunsaturated fatty acid produced by a protein or a combination of proteins of the invention is utilized in an infant formula. In another embodiment, a very long-chain polyunsaturated fatty acid produced by a protein or a combination of proteins of the invention is administered to a subject having a deficiency in very long-chain polyunsaturated fatty acid. In another embodiment, a very long-chain polyunsaturated fatty acid is a polyunsaturated C20 fatty acid.

In another embodiment, the isolated protein comprising desaturase activity is used indirectly or directly in the production of polyunsaturated fatty acids. In another embodiment, the isolated protein or a combination of isolated proteins comprising desaturase and/or desaturase/elongase activities are used indirectly or directly in the production of polyunsaturated fatty acids. In another embodiment, “Directly” is meant to encompass the situation where the enzyme directly desaturates the acid. In another embodiment, the latter of which is utilized in a composition. In another embodiment, “Indirectly” is meant to encompass the situation where an acid is converted to another acid (i.e., a pathway intermediate) by the enzyme and then the latter acid is converted to another acid by use of a non-desaturase enzyme. In another embodiment, a very long-chain polyunsaturated fatty acid produced either directly or indirectly is added to a nutritional composition, pharmaceutical compositions, cosmetics, and animal feeds, all of which are encompassed by the present invention.

In another embodiment, nutritional compositions include any food or preparation for human or animal consumption including for enteral or parenteral consumption, which when taken into the body (a) serve to nourish or build up tissues or supply energy and/or (b) maintain, restore or support adequate nutritional status or metabolic functions. In another embodiment, the nutritional composition of the present invention comprises at least one oil or acid produced directly or indirectly by use of the protein of the invention and may either be in a solid or liquid form. In another embodiment, the composition includes edible macronutrients, vitamins and minerals in amounts desired for a particular use. In another embodiment, the amount of such ingredients will vary depending on whether the composition is intended for use with normal, healthy infants, children or adults having specialized needs such as those which accompany certain metabolic conditions (e.g., metabolic disorders).

In another embodiment, the macronutrients include edible fats, carbohydrates and proteins. In another embodiment, edible fats include but are not limited to coconut oil, soy oil, and mono- and diglycerides. In another embodiment, carbohydrates include but are not limited to glucose, edible lactose and hydrolyzed search. In another embodiment, proteins which are utilized in the nutritional composition of the invention include but are not limited to soy proteins, electrodialysed whey, electrodialysed skim milk, milk whey, or the hydrolysates of these proteins.

In another embodiment, vitamins and minerals are added to the nutritional compositions of the present invention and include but are not limited to: calcium, phosphorus, potassium, sodium, chloride, magnesium, manganese, iron, copper, zinc, selenium, iodine, and Vitamins A, E, D, C, and the B complex. Other such vitamins and minerals may also be added.

In another embodiment, components utilized in the nutritional compositions of the present invention will be of semi-purified or purified origin. By semi-purified or purified is meant a material which has been prepared by purification of a natural material or by synthesis. In another embodiment, nutritional compositions of the present invention include but are not limited to infant formulas, dietary supplements, dietary substitutes, and rehydration compositions. In another embodiment, a nutritional composition of the present invention may also be added to food even when supplementation of the diet is not required. In another embodiment, a composition is added to food of any type including but not limited to margarines, modified butters, cheeses, milk, yogurt, chocolate, candy, snacks, salad oils, cooking oils, cooking fats, meats, fish and beverages.

In another embodiment, a nutritional composition is an enteral nutritional product. In another embodiment, a nutritional composition is an adult or pediatric enteral nutritional product. In another embodiment, a composition is administered to adults or children experiencing stress or having specialized needs due to chronic or acute disease states. In another embodiment, a composition comprises, in addition to polyunsaturated fatty acids produced in accordance with the present invention, macronutrients, vitamins and minerals as described above. In another embodiment, the macronutrients may be present in amounts equivalent to those present in human milk or on an energy basis, i.e., on a per calorie basis.

In another embodiment, the present invention includes an enteral formula comprising polyunsaturated fatty acids produced in accordance with the present invention. In another embodiment, an enteral formula is sterilized and subsequently utilized on a ready-to-feed basis or stored in a concentrated liquid or powder. In another embodiment, a powder is prepared by spray drying the formula prepared as indicated above, and reconstituting it by rehydrating the concentrate. In another embodiment, the present invention includes an adult and pediatric nutritional formulas. In another embodiment, adult and pediatric nutritional formulas are known in the art and are commercially available (e.g., Similac®, Ensure®, Jevity® and Alimentum® from Ross Products Division, Abbott Laboratories). In another embodiment, an oil or acid produce in accordance with the present invention may be add to any of these formulas.

In another embodiment, a nutritional formula comprises macronutrients, vitamins, and minerals, as provided herein, in addition to the PUFAs produced in accordance with the present invention. In another embodiment, the presence of additional components helps the individual ingest the minimum daily requirements of these elements. In another embodiment, an adult and pediatric nutritional formulas comprises the PUFAs as described herein and zinc, copper, folic acid and antioxidants, or any combination thereof. In another embodiment, PUFAs produced in accordance with the present invention, or derivatives thereof, are added to a dietary substitute or supplement, particularly an infant formula, for patients undergoing intravenous feeding or for preventing or treating malnutrition or other conditions or disease states. In another embodiment, PUFAs produced in accordance with the present invention are used to alter, the composition of infant formulas in order to better replicate the PUFA content of human breast milk or to alter the presence of PUFAs normally found in a non-human mammal's milk.

In another embodiment, parenteral nutritional compositions comprising from about 2 to about 30 weight percent fatty acids calculated as triglycerides are encompassed by the present invention. In another embodiment, other vitamins, particularly fat-soluble vitamins such as vitamin A, D, E and L-carnitine are also included. In another embodiment, a preservative such as alpha-tocopherol is added in an amount of about 0.05-0.5% by weight.

In another embodiment, the present invention includes a PUFA produced in accordance with the present invention or host cells containing them, used as animal food supplements to alter an animal's tissue or milk fatty acid composition to one more desirable for human or animal consumption.

In one embodiment, the polypeptides or protein of the present invention can be provided to the individual per se. In one embodiment, the polypeptides or proteins of the present invention can be provided to the individual as part of a pharmaceutical composition where it is mixed with a pharmaceutically acceptable carrier.

In one embodiment, a “pharmaceutical composition” refers to a preparation of one or more of the active ingredients described herein with other chemical components such as physiologically suitable carriers and excipients. The purpose of a pharmaceutical composition is to facilitate administration of a compound to an organism. In one embodiment, “active ingredient” refers to the polypeptide or protein sequence of interest.

In one embodiment, the present invention provides combined preparations. In one embodiment, “a combined preparation” defines especially a “kit of parts” in the sense that the combination partners as defined above can be dosed independently or by use of different fixed combinations with distinguished amounts of the combination partners i.e., simultaneously, concurrently, separately or sequentially. In some embodiments, the parts of the kit of parts can then, e.g., be administered simultaneously or chronologically staggered, that is at different time points and with equal or different time intervals for any part of the kit of parts. The ratio of the total amounts of the combination partners, in some embodiments, can be administered in the combined preparation. In one embodiment, the combined preparation can be varied, e.g., in order to cope with the needs of a patient subpopulation to be treated or the needs of the single patient which different needs can be due to a particular disease, severity of a disease, age, sex, or body weight as can be readily made by a person skilled in the art.

In one embodiment, the phrase “physiologically acceptable carrier” refers to a carrier or a diluent that does not cause significant irritation to a tissue such as a plant tissue or a cell such as a plant cell; and does not abrogate the biological activity and properties of the protein or polynucleotide of the invention. An adjuvant is included under these phrases. In one embodiment, one of the ingredients included in the physiologically acceptable carrier can be for example polyethylene glycol (PEG), a biocompatible polymer with a wide range of solubility in both organic and aqueous media (Mutter et al. (1979).

In one embodiment, “excipient” refers to an inert substance added to the composition to further facilitate administration of an active ingredient. In one embodiment, excipients include calcium carbonate, calcium phosphate, various sugars and types of starch, cellulose derivatives, gelatin, vegetable oils and polyethylene glycols.

Techniques for formulation and administration of peptide to plants or in-vitro are known to one of skill in the art.

In one embodiment, compositions of the present invention are manufactured by processes well known in the art, e.g., by means of conventional mixing, dissolving, or lyophilizing processes.

In one embodiment, compositions for use in accordance with the present invention is formulated in conventional manner using one or more physiologically acceptable carriers comprising excipients and auxiliaries, which facilitate processing of the proteins/polynucleotides into preparations. In one embodiment, formulation is dependent upon the method of administration chosen.

The compositions also comprise, in some embodiments, preservatives, such as benzalkonium chloride and thimerosal and the like; chelating agents, such as edetate sodium and others; buffers such as phosphate, citrate and acetate; tonicity agents such as sodium chloride, potassium chloride, glycerin, mannitol and others; antioxidants such as ascorbic acid, acetylcystine, sodium metabisulfote and others; aromatic agents; viscosity adjustors, such as polymers, including cellulose and derivatives thereof; and polyvinyl alcohol and acid and bases to adjust the pH of these aqueous compositions as needed. The compositions also comprise, in some embodiments, local anesthetics or other actives. The compositions can be used as sprays, mists, drops, and the like.

Additionally, suspensions of the active ingredients, in some embodiments, are prepared as appropriate oily or water based suspensions. Suitable lipophilic solvents or vehicles include, in some embodiments, fatty oils such as sesame oil, or synthetic fatty acid esters such as ethyl oleate, triglycerides or liposomes. Aqueous injection suspensions contain, in some embodiments, substances, which increase the viscosity of the suspension, such as sodium carboxymethyl cellulose, sorbitol or dextran. In another embodiment, the suspension also contains suitable stabilizers or agents, which increase the solubility of the active ingredients to allow for the preparation of highly concentrated solutions.

In another embodiment, the proteins as described herein can be delivered in a vesicle, in particular a liposome (see Langer, Science 249:1527-1533 (1990); Treat et al., in Liposomes in the Therapy of Infectious Disease and Cancer, Lopez-Berestein and Fidler (eds.), Liss, N.Y., pp. 353-365 (1989); Lopez-Berestein, ibid., pp. 317-327; see generally ibid).

In some embodiments, the protein as described herein is in powder form for constitution with a suitable vehicle, e.g., sterile, pyrogen-free water based solution, before use. In another embodiment, compositions are contained in a container with attached atomizing means.

In some embodiments, compositions suitable for use in context of the present invention include compositions wherein the proteins or oligonucleotides are contained in an amount effective to achieve the intended purpose. In one embodiment, determination of the effective amount is well within the capability of those skilled in the art.

Some examples of substances which can serve as carriers or components thereof are sugars, such as lactose, glucose and sucrose; starches, such as com starch and potato starch; cellulose and its derivatives, such as sodium carboxymethyl cellulose, ethyl cellulose, and methyl cellulose; powdered tragacanth; malt; gelatin; talc; solid lubricants, such as stearic acid and magnesium stearate; calcium sulfate; vegetable oils, such as peanut oil, cottonseed oil, sesame oil, olive oil, corn oil and oil of theobroma; polyols such as propylene glycol, glycerine, sorbitol, mannitol, and polyethylene glycol; alginic acid; emulsifiers, such as the Tween brand emulsifiers; wetting agents, such sodium lauryl sulfate; coloring agents; flavoring agents; tableting agents, stabilizers; antioxidants; preservatives; pyrogen-free water, isotonic saline; and phosphate buffer solutions. The choice of a pharmaceutically-acceptable carrier to be used in conjunction with the compound is basically determined by the way the compound is to be administered. If the subject compound is to be injected, in one embodiment, the pharmaceutically-acceptable carrier is sterile, physiological saline, with a blood-compatible suspending agent, the pH of which has been adjusted to about 7.4.

In addition, the compositions further comprise binders (e.g., acacia, cornstarch, gelatin, carbomer, ethyl cellulose, guar gum, hydroxypropyl cellulose, hydroxypropyl methyl cellulose, povidone), disintegrating agents (e.g., cornstarch, potato starch, alginic acid, silicon dioxide, croscarmelose sodium, crospovidone, guar gum, sodium starch glycolate), buffers (e.g., Tris-HCl, acetate, phosphate) of various pH and ionic strength, additives such as albumin or gelatin to prevent absorption to surfaces, detergents (e.g., Tween 20, Tween 80, Pluronic F68, bile acid salts), protease inhibitors, surfactants (e.g., sodium lauryl sulfate), permeation enhancers, solubilizing agents (e.g., glycerol, polyethylene glycerol), anti-oxidants (e.g., ascorbic acid, sodium metabisulfite, butylated hydroxyanisole), stabilizers (e.g., hydroxypropyl cellulose, hyroxypropylmethyl cellulose), viscosity increasing agents(e.g., carbomer, colloidal silicon dioxide, ethyl cellulose, guar gum), sweeteners (e.g., aspartame, citric acid), preservatives (e.g., Thimerosal, benzyl alcohol, parabens), lubricants (e.g., stearic acid, magnesium stearate, polyethylene glycol, sodium lauryl sulfate), flow-aids (e.g., colloidal silicon dioxide), plasticizers (e.g., diethyl phthalate, triethyl citrate), emulsifiers (e.g., carbomer, hydroxypropyl cellulose, sodium lauryl sulfate), polymer coatings (e.g., poloxamers or poloxamines), coating and film forming agents (e.g., ethyl cellulose, acrylates, polymethacrylates) and/or adjuvants.

The compositions also include incorporation of the proteins or oligonucleotides of the invention into or onto particulate preparations of polymeric compounds such as polylactic acid, polglycolic acid, hydrogels, etc., or onto liposomes, microemulsions, micelles, unilamellar or multilamellar vesicles, erythrocyte ghosts, or spheroplasts.) Such compositions will influence the physical state, solubility, stability, rate of in vivo release, and rate of in vivo clearance.

Also comprehended by the invention are particulate compositions coated with polymers (e.g. poloxamers or poloxamines) and the proteins or oligonucleotides of the invention coupled to antibodies directed against tissue-specific receptors, ligands or antigens or coupled to ligands of tissue-specific receptors.

In some embodiments, the proteins or oligonucleotides of the invention modified by the covalent attachment of water-soluble polymers such as polyethylene glycol, copolymers of polyethylene, glycol and polypropylene glycol, carboxymethyl cellulose, dextran, polyvinyl alcohol, polyvinylpyrrolidone or polyproline. In another embodiment, the modified proteins or oligonucleotides of the invention exhibit substantially longer half-lives in blood following intravenous injection than do the corresponding unmodified compounds. In one embodiment, modifications also increase the proteins or oligonucleotides solubility in aqueous solution, eliminate aggregation, enhance the physical and chemical stability of the compound, and greatly reduce the immunogenicity and reactivity of the compound. In another embodiment, the desired in vivo biological activity is achieved by the administration of such polymer-compound abducts less frequently or in lower doses than with the unmodified compound.

Additional objects, advantages, and novel features of the present invention will become apparent to one ordinarily skilled in the art upon examination of the following examples, which are not intended to be limiting. Additionally, each of the various embodiments and aspects of the present invention as delineated hereinabove and as claimed in the claims section below finds experimental support in the following examples.

EXAMPLES

Generally, the nomenclature used herein and the laboratory procedures utilized in the present invention include molecular, biochemical, microbiological and recombinant DNA techniques. Such techniques are thoroughly explained in the literature. See, for example, “Molecular Cloning: A laboratory Manual” Sambrook et al., (1989); “Current Protocols in Molecular Biology” Volumes I-III Ausubel, R. M., ed. (1994); Ausubel et al., “Current Protocols in Molecular Biology”, John Wiley and Sons, Baltimore, Maryland (1989); Perbal, “A Practical Guide to Molecular Cloning”, John Wiley & Sons, New York (1988); Watson et al., “Recombinant DNA”, Scientific American Books, New York; Birren et al. (eds) “Genome Analysis: A Laboratory Manual Series”, Vols. 1-4, Cold Spring Harbor Laboratory Press, New York (1998); methodologies as set forth in U.S. Pat. Nos. 4,666,828; 4,683,202; 4,801,531; 5,192,659 and 5,272,057; “Cell Biology: A Laboratory Handbook”, Volumes I-III Cellis, J. E., ed. (1994); “Culture of Animal Cells—A Manual of Basic Technique” by Freshney, Wiley-Liss, N.Y. (1994), Third Edition; “Current Protocols in Immunology” Volumes I-III Coligan J. E., ed. (1994); Stites et al. (eds), “Basic and Clinical Immunology” (8th Edition), Appleton & Lange, Norwalk, Conn. (1994); Mishell and Shiigi (eds), “Selected Methods in Cellular Immunology”, W. H. Freeman and Co., New York (1980); available immunoassays are extensively described in the patent'and scientific literature, see, for example, U.S. Pat. Nos. 3,791,932; 3,839,153; 3,850,752; 3,850,578; 3,853,987; 3,867,517; 3,879,262; 3,901,654; 3,935,074; 3,984,533; 3,996,345; 4,034,074; 4,098,876; 4,879,219; 5,011,771 and 5,281,521; “Oligonucleotide Synthesis” Gait, M. J., ed. (1984); “Nucleic Acid Hybridization” Hames, B. D., and Higgins S. J., eds. (1985); “Transcription and Translation” Hames, B. D., and Higgins S. J., eds. (1984); “Animal Cell Culture” Freshney, R. I., ed. (1986); “Immobilized Cells and Enzymes” IRL Press, (1986); “A Practical Guide to Molecular Cloning” Perbal, B., (1984) and “Methods in Enzymology” Vol. 1-317, Academic Press; “PCR Protocols: A Guide To Methods And Applications”, Academic Press, San Diego, Calif. (1990); Marshak et al., “Strategies for Protein Purification and Characterization—A Laboratory Course Manual” CSHL Press (1996); all of which are incorporated by reference. Other general references are provided throughout this document.

Experimental Procedures Strains And Growth Conditions

Axenic cultures of P. incisa were cultivated on BG-11 nutrient medium in 250 ml Erlenmeyer glass flasks in an incubator shaker at controlled temperature (25° C.) and illumination (115 μmol quanta m⁻² S⁻¹) under an air/CO₂ atmosphere (99:1, v/v) and a speed of 170 rpm. For N-starvation experiments, cells of daily-diluted cultures were collected by centrifugation, washed three times in sterile DDW and resuspended in N-free BG11 medium. To prepare N-free BG-11 medium, sodium nitrate was omitted and ferric ammonium citrate was substituted with ferric citrate. Biomass was sampled at time 0, and in 1.5, 3, 7 and 14 days from the onset of N-starvation for determination of growth parameters, and was further used for fatty acid analysis and RNA isolation. Duplicate samples were collected from 3 separate flasks for each time point and measurement.

Growth Parameters

Dry weight and chlorophyll contents were determined as previously described in A. E. Solovchenko, I. Khozin-Goldberg, Z. Cohen, M. N. Merzlyak, Carotenoid-to-chlorophyll ratio as a proxy for assay of total fatty acids and arachidonic acid content in the green micro-alga, Parietochloris incisa, J. Appl. Phycol. (2008) 361-366.

RNA Isolation

Aliquots of the cultures were filtered through a glass fiber filter (GF-52, Schleicher & Schuell, Germany); cells were collected by scraping and immediately flash-frozen in liquid nitrogen and stored at −80° C. for further use. Total RNA was isolated by the procedure described by Bekesiova et al. (I. Bekesiova, J. P. Nap, L. Mlynarova, Isolation of high quality DNA and RNA from leaves of the carnivorous plant Drosera rotundifolia, Plant. Mol. Biol. Rep. 17 (1999) 269-277), with minor modifications. Three independent RNA isolations were conducted for each time point. The total RNA samples were treated with RNAase-free Baseline-ZERO™ DNAase (Epicentre Technologies, Madison, Wis., USA) before being used in cDNA synthesis for real-time PCR experiments.

Gene Cloning

Partial sequences of the Δ12, Δ6, Δ5 desaturase and actin genes were obtained by PCR (ReddyMix PCR Master Mix, Thermo Scientific, Surrey, UK) using the degenerated primers listed in the Table 1. To generate the full-length cDNAs, 3′- and 5′-rapid amplification of the cDNA ends (RACE) was performed using a BD Smart™ RACE cDNA Amplification Kit (BD Biosciences Clontech, Foster City, Calif., USA). Gene specific primers were designed (Table 1) and RACE PCR reactions were conducted using 5′ and 3′-RACE-Ready cDNAs made from 1 μg total RNA of N-starved cells with 50× BD Advantage 2 polymerase mix (Clontech Laboratories Inc., Mountain View, Calif., USA). The PCR products of the expected sizes were excised, purified from the gel (Nucleo Spin Extract II purification kit, Machery-Nagel, Duren, Germany) and ligated into a pGEM T-Easy vector (Promega, Madison, Wis., USA). The full-length cDNAs were assembled based on the sequences of the 5′ and 3′ RACE fragments.

TABLE 1 Primers used for obtaining partial, 5′ and 3′ end fragments of actin, Δ12, A6 and A5 desaturase genes of P. incisa followed by full-length assembly SEQ ID Gene Forward/Reverse primer (Sequence 5′ to 3′) NO: Primers used for partial sequence DesΔ12 CAC MYC VTS THC VWG CTG CTG VWB CCC CAC (FWD) 9 CTG CCC GAA GTT GAC CGC GGC GTG CTG (REV) 10 DesΔ6 TGG TGG AAR CAY AAR CAY AAY (FWD) 11 GCG AGG GAT CCA AGG RAA NAR RTG RTG YTC (REV) 12 DesΔ5 ATH RAI GRI AAR GTI TAY GAY GT (FWD) 13 GGI AYI KWI TSD ATR TCI GGR TC (REV) 14 Actin AGA TCT GGC ACC ACA CCT TCT TCA (FWD) 15 TGT TGT TGT AGA GGT CCT TGC GGA (REV) 16 Primers used for 5′ and 3′ RACE amplification DesΔ12 CCACATAGCGGCACAGGCTGAAATC (FWD) 17 GCTCTGGGAGGATTTCAGCCTGTGC (REV) 18 DesΔ6 GACACAATCTGGGCCGTCACAAAGTC (FWD) 19 GGACTTTGTGACGGCCCAGATTGTGTC (REV) 20 DesΔ5 ACTGACCCTCCTCTGTGTCCTCTTCG (FWD) 21 TGTACGCCAAGTCGCTGACCATCC (REV) 22 Restriction sites*/ SEQ ID Primers used for full-length cloning and yeast transformations NO: DesΔ12 TGGAATTC AAAATGGGGAAAGGAGGCTG (FWD) EcoRI/23 CTGTCTAGA TCAAGCGCGGAACCACAGG Xba I/24 DesΔ6 TCGAATTCAAAATGTGCCAGGGACAGG (FWD) EcoRI/25 GGCTCTAGA CTAGGCCTCAGCTGCCACG XbaI/26 DesΔ5 CCAAAGCTTAAAATGATGGCTGTAACAGA (FWD) HindIII/27 GCTCTAGA CTATCCCACGGTGGCCA XbaI/28

Expression And Functional Characterization In the Yeast Saccharomyces Cerevisiae

The open reading frames (ORFs) encoding for the Δ2, Δ6, and Δ5 desaturases were amplified using PfuUltra II fusion HS DNA polymerase (Stratagene, La Jolla, Calif., USA) with the respective primer pairs (Table 1). The forward primers contained a restriction site (underlined) and a yeast translation consensus (double underlined) followed by ATG. The reverse primers contained a restriction site (underlined) and a stop codon (double underlined). Following restriction and ligation to the pYES2 vector (Invitrogen, Carlsbad, Calif., USA), the constructs were used to transform S. cerevisiae strain W303 by the PEG/lithium acetate method [R. D. Gietz, R. A. Woods, Yeast Transformation by the LiAc/SS Carrier DNA/PEG Method, in: W. Xiao (Ed.), Yeast Protocols, Second Edition, vol. 313, Methods in Molecular Biology, Humana Press Inc, Totowa, N.J., 2006, pp.107-120]. The yeast cells harboring the empty pYES2 vector were used as control. Transformants were selected by uracil prototrophy on yeast synthetic medium (YSM) lacking uracil (Invitrogen, Carlsbad, Calif., USA). For functional expression, a minimal selection medium containing 2% (w/v) raffinose was inoculated with the pYPiDesΔ12, pYPiDesΔ6 or pYPiDesΔ5 transformants and grown at 27° C. for 24 h in a water bath shaker. Five ml of sterile YSM, containing 1% (w/v) Tergitol-40 and 250 μM of the appropriate fatty acid substrate was inoculated with raffinose-grown cultures to obtain an OD of 0.2 at 600 nm. Expression was induced by adding galactose to a final concentration of 2% (w/v) and cultures were further grown at 27° C. for 48 h. Cells were harvested by centrifugation, washed twice with 0.1% NaHCO₃, freeze-dried and used for fatty acid analysis.

Generation of 5′ And 3′ End Fragments of the Putative P. Incisa PUFA Elongase

To generate the full-length cDNA of the putative PUFA elongase, 3′-and 5′-rapid amplification of the cDNA ends (RACE) was performed using a BD smart™ RACE cDNA Amplification Kit (BD Biosciences Clontech, Foster City, Calif.) according to the manufacturer's manual. To amplify the 5′-end, the reverse gene-specific primers (GSP) 5′-CCCGGCTGCTGCCATGCTTCTGTG (EL5R1) (SEQ ID NO: 29) 5′-TGGGGTAGGGAGAGTAGGCCCAAGT (EL5RN) (SEQ ID NO: 30) were designed using the Primer3 online software (http://frodo.wi.mit.edu). Based on the nucleotide sequence of the obtained 5′-end fragment, two forward GSPs, 5′-GCCTACATGTCCTCTGCCGCCTGCTA (EL3R1) (SEQ ID NO: 31) and the nested, 5′-GCGGGACATGGGAGGGCTCATCTATACC (EL3R2) (SEQ ID NO: 32), were constructed to amplify the 3′-end of the target gene. RACE PCR reactions were conducted using 5′ and 3′-RACE-Ready cDNAs made from lug total RNA of N-starved cells with 50× BD Advantage 2 polymerase mix (Clontech Laboratories Inc., Mountain View, Calif.). The PCR products of the expected size were excised and purified from the gel (NucleoSpin Extract II purification kit, Machery-Nagel, Duren, Germany) and ligated into a pGEM T-Easy vector (Promega, Madison, Wis.). The full length cDNA corresponding to the P. incisa putative PUFA elongase (designated PiELO1) was assembled from the 5′ and 3′ RACE fragments and its ORF was further subcloned into a pYES2 vector (Invitrogen, Carlsbad, Calif.).

Expression And Functional Characterization of PiELO1 cDNA (Elongase) In the Yeast Saccharomyces Cerevisiae

The ORF encoding for PiELO1 was amplified using PfuUltra II fusion HS DNA polymerase (Stratagene, La Jolla, Calif.) with the forward primer, 5′-AGGAATTCAAAATGGCATTGACGGCGGCCT (PUFAEL5RES1) (SEQ ID NO: 33), containing a restriction site (underlined) and a yeast translation consensus followed by ATG (double underlined) and the reverse primer 5′-CATTCTAGATTACTGCAGCTTTTGCTTGGCTGC (PUFAEL3RES2) (SEQ ID NO: 34) containing a restriction site (underlined) and a stop codon (double underlined). The amplified sequence was then restricted with EcoRI and XbaI (NEB, Ipswich, Mass.). The expected bands were gel-purified with NucleoSpin Extract II purification kit (Machery-Nagel GmbH, Duren, Germany) and ligated into a EcoRI-Xbal cut pYES2 vector, yielding YpPiELO1. Saccharomyces cerevisiae strain W303 was transformed with YpPiELO1 by the PEG/lithium acetate method. The yeast cells harboring the empty pYES2 vector were used as control. Transformants were selected by uracil prototrophy on yeast synthetic medium (YSM) lacking uracil (Invitrogen, Carlsbad, Calif.). For functional expression, a minimal selection medium containing 2% (w/v) raffinose was inoculated with the YpPiELO1-transformants and grown at 27° C. for 24 h in a water bath shaker. Five ml of sterile YSM, containing 1% (w/v) Tergitol-40 and 250 μM of the appropriate fatty acid was inoculated with raffinose-grown cultures to obtain an OD of 0.2 at 600 nm. Expression was induced by adding galactose to a final concentration of 2% (w/v) and cultures were further grown at 27° C. for 48 h. Cells were harvested by centrifugation, washed twice with 0.1% NaHCO₃, freeze-dried and used for fatty acid analysis.

Primer Design And Validation For PiELO1 (Elongase)

Real-Time Quantitative PCR primer pairs were designed for the PiELOJ and the house keeping gene 18S SSU rRNA using the PrimerQuest tool (http://test.idtdna.com/Scitools/Applications/Primerquest/). Parameters were set for a primer length of 19 to 26 bp, primer melting temperature of 60.0±1.0° C., and amplicon length of 90 to 150 bases. Primer pairs were validated using seven serial fifty-fold dilutions of cDNA samples and standard curves were plotted to test for linearity of the response. The primer pairs and primer concentrations with reaction efficiencies of 100±10% were chosen for quantitative RT-PCR analysis of relative gene expression. The nucleotide sequences and characteristics of primers used for quantitative RT-PCR analysis are presented in Table 2.

TABLE 2 Parameters of the primers used in RTQPCR reactions Amplicon PCR Forward primer size efficiency Gene Reverse primer (bp) (%) PiELO1 AAGCTGTACGAGTTTGTGGATACGCT (SEQ ID NO: 35) (FWD) 95 92.3 GGATATGGAAGCGTGGTGGTAGA (SEQ ID NO: 36) (REV) 18S TGAAAGACGAACTTCTGCGAAAGCA (SEQ ID NO: 37) (FWD) 120 96.8 SSU AGTCGGCATCGTTTATGGTTGAGA (SEQ ID NO: 38) (REV) rRNA

Calculation of Gene Transcript Levels

The mean fold changes in gene expression were calculated according to the 2^(-ΔΔCt) method using the average of threshold cycle (Ct) values from triplicate cDNA-primer samples. The ACt followed by the AACt was calculated from the average Ct values of the target and the endogenous genes. The transcript abundance of the PiELO1 gene was normalized to the endogenous control 18S SSU rRNA gene. The fold-change in gene expression was calculated using 2^(-ΔΔCt) to find the expression level of the target gene which was normalized to the endogenous gene, relative to the expression of the target gene at time 0.

Fatty Acid Analysis

Fatty acid methyl esters (FAMES) were obtained by transmethylation of the freeze-dried P. incisa or yeast biomass, with dry methanol containing 2% H₂SO4 (v/v) and heating at 80° C. for 1.5 h while stirring under an argon atmosphere. Gas chromatographic analysis of FAMEs was performed on a Thermo Ultra Gas chromatograph (Thermo Scientific, Italy) equipped with PTV injector, FID detector and a fused silica capillary column (30 m×0.32 mm; ZB WAXplus, Phenomenex). FAMEs were identified by co-chromatography with authentic standards (Sigma Chemical Co., St. Louis, Mo.; Larodan Fine Chemicals, Malmö, Sweden) and FAME of fish oil (Larodan Fine Chemicals). Each sample was analyzed in duplicates of three independent experiments. The structures of fatty acids were confirmed by GC-MS of their pyrrolidine derivatives [W.W. Christie, The analysis of fatty acids in: W.W. Christie (Ed.), Lipid analysis Isolation, separation, identification and structural analysis of lipids, vol. 15, Third edition, The Oily Press, Bridgewater, England, 2003, pp. 205-225] on HP 5890 equipped with a mass selective detector (HP 5971A) utilizing a HP-5 capillary column and a linear temperature gradient from 120 to 300° C.

Lipid Analysis

The biomass of S. cerevisiae was heated with isopropanol at 80° C. for 10 min and lipids were extracted by the method of Bligh-Dyer (1959) [E. G. Bligh, W. J. Dyer, A rapid method of total lipid extraction and purification, Can. J. Biochem. Physiol. 37 (1959) 911-917]. Total lipid extract was separated into neutral and polar lipids by silica Bond-Elute cartridges (Varian, Calif.) using 1% of ethanol in chloroform (v/v) and methanol to elute neutral and polar lipids, respectively [Z. Cohen, S. Didi, Y. M. Heimer, Overproduction of γ-linolenic and eicosapentaenoic acids by algae, Plant Physiol. 98 (1992) 569-572].

Polar lipids were separated into individual lipids by two dimensional TLC on Silica Gel 60 glass plates (10×10 cm, 0.25 mm thickness (Merck, Darmstadt, Germany) according to Khozin et al. [I. Khozin, D. Adlerstein, C. Bigogno, Y. M. Heimer, Z. Cohen, Elucidation of the Biosynthesis of Eicosapentaenoic Acid in the Microalga Porphyridium cruentum (II. Studies with Radiolabeled Precursors), Plant Physiol. 114 (1997) 223-230]. Neutral lipids were resolved with petroleum ether:diethyl ether:acetic acid (70:30:1, v/v/v). Lipids on TLC plates were visualized by brief exposure to iodine vapors, scraped from the plates and were transmethylated for the fatty acid analysis as previously described.

Real-Time Quantitative PCR

Template cDNA for real-time quantitative PCR (RTQPCR) was synthesized using 1 μg of total RNA in a total volume of 20-μl, using oligo dT primer (Reverse-iT TM 1^(st) Strand Synthesis Kit, ABgene, Surrey, UK). Each 20-μL cDNA reaction was then diluted 3-fold with PCR grade water.

Primer Design And Validation For Real-Time Quantitative PCR

Real-Time Quantitative PCR (RTQPCR) primer pairs were designed for the PiDes12, PiDes6, and PiDes5 genes and the house keeping gene actin, PiAct using the PrimerQuest tool (http://test.idtdna.com/Scitools/Applications/Primerquest/). Primer pairs were validated as described by Iskandarov et al. [U. Iskandarov, I. Khozin-Goldberg, R. Ofir, Z. Cohen, Cloning and Characterization of the Δ6 Polyunsaturated Fatty Acid Elongase from the Green Microalga Parietochloris incisa, Lipids 44 (2009) 545-554]. The nucleotide sequences of primer pairs and the amplicon sizes are presented in Table 3.

TABLE 3 Primers used in RTQPCR experiments Forward primer/ Amplicon Gene Reverse primer size (bp) PiDes12 5′-GAAGCACCACCAAGGATGAGGT (SEQ ID NO: 39) (FWD) 112 5′-AGCGAGACGAAGATGACCAGGAA (SEQ BD NO: 40) (REV) PiDes6 5′-ACTTCCTGCACCACCAGGTCTTC (SEQ ID NO: 41) (FWD) 112 5′-TCGTGCTTGCTCTTCCACCAGT (SEQ ID NO: 42) (REV) PiDes5 5′-TAAGTGCCAGGGCTGTGCTAGA (SEQ ID NO: 43) (FWD) 110 5′-GAACTGACCCTCCTCTGTGTCCT (SEQ ID NO: 44) (REV) PiAct 5′-CGTCCAGCTCCACGATTGAGAAGA (SEQ ID NO: 45) (FWD) 154 5′-ATGGAGTTGAAGGCGGTCTCGT (SEQ ID NO: 46) (REV)

Example 1 Isolation And Identification of CDNAS For Δ12, Δ6, And Δ5 Desaturase Genes of P. Incisa

The partial sequences of the Δ12, Δ6 and Δ5 desaturase gene homologues were isolated using degenerate oligonucleotides (Table 1) targeting conserved amino acid motifs identified in algae, lower plants and fungi. A partial sequence of the actin gene was amplified to be used as a house keeping gene in RTQPCR experiments.

Partial sequences of 503, 558 and 636 bp, corresponding to the Δ12, Δ6, and Δ5 desaturase genes, respectively, were used for designing gene specific primers that were used to amplify the 5′- and 3′-ends of the expected genes. Assembling the 5′ and 3′ RACE PCR product sequences resulted in the identification of three cDNA clones with sequence homologies to known Δ12, Δ6, and Δ5 desaturase genes. The full-length cDNAs corresponding to Δ12, Δ6, and Δ5 desaturase genes were thus designated PiDes12, PiDes6, and PiDes5. The ORFs for PiDes12, PiDes6 and PiDes5 genes were 1140, 1443, and 1446 by in length, respectively, coding for the corresponding predicted proteins of 380, 481 and 482 amino acids. The predicted amino acid sequence of PiDes12 is 64% and 62% identical to that of Chlorella vulgaris (BAB78716) and Chlamydomonas reinhardtii (XP_(—)001691669), respectively, while it shares more than 50% identity with those of higher plants. It contains three conserved histidine motifs HxxxH, HxxHII and HxxHH. The deduced amino acid sequence of PiDes6 is 52% and 51% identical to those of the Δ6 desaturases from the liverwort M. polymorpha (AAT85661) and the moss Ceratodon purpureus, respectively (CAB94993). It is also 45% identical to the M. alpina Δ6 desaturase (ABN69090). PiDes5 shares 55 and 51% identity with the Δ5 desaturase from the microalgae M. squamata (CAQ30478), and O. tauri (CAL57370), respectively, and 54% with that from M. polymorpha (AAT85663) but is only 36% identical to the M. alpina Δ5 desaturase (AAC72755). Both PiDes6 and PiDes5 contain N-terminal fused cytochrome b5 domain including the HPGG motif and the three histidine boxes found to be conserved in front-end desaturases. The three characteristically conserved histidine-rich motifs with amino acid patterns of HD_((E))xxH, HxxHH,, QxxHH in Δ6 desaturases, and HDxxH, QHxxxHH, QxxHH in Δ5 desaturases are also present in PiDes6 and PiDes5, respectively (FIG. 1).

Phylogenetic Analysis

An unrooted phylogenetic tree (FIG. 2) of PiDes12, PiDes6, PiDes5 and several functionally characterized desaturases from all three groups were constructed to identify their functional and phylogenetic relationships by the neighbor-joining program in MEGA4 [K. Tamura, J. Dudley, M. Nei, S. Kumar, MEGA4: Molecular evolutionary genetics analysis (MEGA) software version 4.0, Mol. Biol. Evol. 24 (2007) 1596-1599]. The deduced amino acid sequence of PiDes12 is closely related to Δ12 desaturases of green algae and very similar to those of higher plants. The sequences of PiDes6 and PiDes5 cluster with Δ6 and Δ5 desaturases, respectively, from algae, moss and fungi. PiDes6 is highly similar to the M. polymorpha (MpDEs6) and P. tricornutum (PtD6p) Δ6 desaturases, while PiDes5 appears to be closely related to the Δ5 desaturase from the moss M. polymorpha and shares more sequence similarity with the Δ5 desaturase from the chlorophytes M. squamata and O. tauri than with those of fungal origin. However, both Δ6 or Δ5 desaturases from M. squamata and O. tauri appear to be structurally more similar to each other than to any of the known desaturases from either group.

Example 2 Functional Expression of PiDes12, PiDes6, And PiDes5 In S. Cerevisiae

The functional activities of the proteins encoded by PiDes12, PiDes6 and PiDes5 were examined by heterologous expression in S. cerevisiae. To this aim, the pYES2 constructs pYPiDes12, pYPiDes6 and pYPiDes5 containing the ORFs for PiDes12, PiDes6, and PiDes5, respectively, were transformed into S. cerevisiae. GC analysis of the FAMEs of the yeast transformed with pYPiDes12, revealed an appearance of a small peak corresponding to 18:2 (0.3% of TFA; not shown). An attempt to improve the expression of the recombinant protein and to increase the activity by the modification of yeast translation consensus was not successful. The yeast cells harboring the empty vector, pYES2 (control) did not demonstrate desaturation activity on the added substrates (FIG. 3).

PiDes6 and PiDes5 expressions were induced in the presence of the main ω6 substrates for Δ6 or Δ5 fatty acid desaturases, 18:2ω6 and 20:3ω6, respectively. New peaks corresponding to 18:3ω6 and 20:4ω6, respectively, were detected, confirming the predicted function of PiDes6 and PiDes5. The expression of PiDes6 in the presence of 18:3ω3 resulted in the appearance of the corresponding Δ6 desaturation product 18:4ω3 (FIG. 3). PiDes6 desaturase was neither active on endogenous yeast fatty acids nor on external 18:1. PiDes6 was not active on 20:36ω3 either, whereas PiDes5 desaturated it to the non-methylene-interrupted 20:4^(Δ5,11,14,17). PiDes5 converted 20:4ω3 into the respective Δ5 product, 20:5ω3 (EPA) as well as the added 18:1 into the non-methylene-interrupted 18:2^(Δ5,9) (FIG. 3). The Δ5 position on 18:2^(Δ5,9) was determined by a characteristic peak of m/z=180 on the GC-MS spectra of its pyrrolidine derivative (not shown). The presence of 18:2^(Δ5,9) was also observed in the chromatograms of the PiDes5 transformant supplied with C20 fatty acids. In addition, a tiny peak, tentatively identified as 18:4^(Δ5,9,12,15) was present on the chromatogram of the PiDes5 transformant fed with 18:30 (Table 4).

TABLE 4 Conversion percent of the supplied fatty acids by PiDes6 and PiDes5 in S. cerevisiae Fatty acid Desaturase product and conversion (%)* substrate PiDesΔ6 PiDesΔ5 18:1^(Δ9) — 18:2^(Δ5, 9) (4.2) 18:2^(Δ9, 12) 18:2^(Δ6, 9, 12) (5.1) — 18:3^(Δ9, 12, 15) 18:4^(Δ6, 9, 12, 15) (4.5) 18:4^(Δ5, 9, 12, 15)** (1.4) 18:3^(Δ6, 9, 12) — 20:3^(Δ11, 14, 17) — 20:4^(Δ5, 11, 14, 17) (10.0) 20:3^(Δ8, 11, 14) — 20:4^(Δ5, 8, 11, 14) (16.4) 20:4^(Δ8, 11, 14, 17) 20:5^(Δ5, 8, 11, 14, 17) (17.1) *calculated as the ratio of product/(substrate + product) **tentative identification

A kinetic analysis of ARA emergence was conducted in total fatty acids of the PiDes5 transfomiant during 24 h following the addition of DGLA. Results showed that ARA peak was evident already after 3 h (corresponding to 10.9% substrate conversion) with a gradual but slow increase (up to 15.1% conversion) after 24 h. Fatty acid analysis of the major polar and neutral lipids of the yeast transformed with pYPiDes5 was performed 24 h after feeding with 20:3ω6 to study the pattern of distribution of ARA within individual lipids. In the transformed yeast, ARA appeared in all major phospholipids (Table 4), with the highest proportion detected in PC. It was also present in the neutral lipids, TAG, free fatty acids (FFA), diacylglycerol (DAG) and sterol esters (SE). Taking into account that PC, a major phospholipid of S. cerevisiae, constituted for about 16% of total lipids (Table 5), it is obvious that PC allocated the main part of ARA attached to phospholipids.

TABLE 5 Fatty acid composition and distribution of individual lipid classes of S. cerevisiae expressing the PiDes5 ORF. Fatty acid composition (% of total fatty acids) % % 20:4ω6 Lipid 16:0 16:1 18:0 18:1ω9 18:2^(Δ5, 9) 20:3ω6 20:4ω6 conversion of TL* % TL TAG 17.4 27.6 9.6 23.0 0.4 19.6 2.0 9.3 61.3 55.2 SE 10.5 38.5 7.1 30.4 0.0 12.2 1.1 8.4 3.6 1.8 DAG 27.9 16.3 21.9 24.3 0.1 7.2 2.0 24.0 1.6 1.4 FFA 26.1 20.3 23.5 8.9 0.2 17.2 3.6 17.2 5.5 9.1 PC 19.7 30.1 9.3 24.3 0.7 11.6 3.6 24.2 15.7 25.7 PE 21.7 34.9 2.8 32.8 0.5 5.0 1.6 24.6 3.2 2.3 PI + PS 34.0 20.8 12.4 26.5 0.2 4.6 1.1 18.1 9.0 4.4 *TL—total lipids

Example 3 Expression Profiles of PiDes12, PiDes6, And PiDes5 Under Nitrogen Starvation

To use actin as a house-keeping gene in quantitative real-time PCR experiments, a partial fragment (503 bp) of the P. incisa actin gene was amplified using the primers whose design was based on the C. reinhardtii actin cDNA (XM_(—)001699016). Indeed, the expression level of the actin gene did not significantly change throughout the nitrogen starvation. PiDes12, PiDes6, and PiDes5 were upregulated following the transfer to Nitrogen starvation, reaching the highest expression level on day 3 and decreasing thereafter to a level about 15 to 20 fold higher than that at time 0 (FIG. 4). Both the PiDes12 and PiDes5 genes were expressed at levels approximately 65 to 70 fold higher on day 3 than at time 0, while the PiDes6 transcript was about 45 fold higher (FIG. 4). The expression patterns of PiDes12, PiDes6, and PiDes5 correlated with the enhanced biosynthesis of ARA in P. incisa cells (Table 6).

TABLE 6 Major fatty acid composition of P. incisa cells grown under N-starvation Time Fatty acid composition (% of total fatty acids) TFA (d) 16:0 16:1 16:2 16:3 18:0 18:1 18:2 18:3ω6 18:3ω3 20:3ω6 20:4ω6 20:5ω3 (% DW) 0 19.1 5.6 4.1 2.9 3.1 9.1 20.1 1.2 6.0 0.5 23.0 0.7 6.4 1.5 15.9 3.1 2.3 2.1 3.8 15.6 15.6 2.1 2.9 1.0 30.3 0.6 8.7 3 12.7 2.3 1.5 1.9 3.8 15.2 13.5 1.6 2.0 0.9 39.7 0.6 11.0 7 10.7 1.0 0.6 1.1 3.5 14.9 10.0 1.1 0.9 1.0 50.0 0.5 21.2 14 9.0 0.2 0.3 0.8 3.1 13.4 8.8 0.9 0.6 0.9 56.9 0.6 29.0

Example 4 Identification And Characterization of PiELO1

The BLASTX analysis (http://www.ncbi.nlm.nih.gov/blast) of clones obtained through subtractive hybridization revealed a clone of 141 bp whose putative amino acid sequence was highly homological to the C-terminal region of PUFA elongases. Using GSP primers, the 870 by 5′-end fragment was amplified and the sequence information was used to obtain the 3′ end fragment from the 3′ RACE Ready cDNA. Alignment of the 800 by 3′-end sequence with that of the 5′-end fragment provided an overlapping nucleotide sequence and included the partial 141 bp sequence, thus confirming the amplification of both ends of the expected gene. The assembled complete 867 by cDNA sequence, designated as PiELO1, preceded and followed by 22 and 150 by nucleotides at 5′ and 3′ UTR, respectively. PiELO1 contained an ORF of 289 predicted amino acid residues consistent with functionally characterized PUFA elongase ORFs from fungi, lower plants and algae (FIG. 5). The deduced amino acid sequence of the PiELO1 was 50% identical to O. tauri and M. polymorpha Δ6 PUFA elongase, while sharing 48 and 44% identity with P. patens Δ6 elongase and M. polymorpha Δ5 elongase, respectively. The PiELO1 is also similar, yet with a lower score, to Δ6 elongases of fungal origin. It shares 40 and 36% identity with the Δ6 PUFA elongases of Thraustochytrium and M. alpina (not included in the alignment), respectively.

The predicted amino acid sequence of the PiELO1 contained four conserved motifs that are characteristic for PUFA elongases (FIG. 5, highlighted). The hydropathy plot of the PiELO1 deduced amino acid sequences was obtained using the algorithm available in the DAS transmembrane prediction server (http://www.sbc.su.se/˜miklos/DAS/). The two strictly hydrophobic transmembrane domains were found about 50 amino acids downstream and upstream from the N and C termini, respectively, while the two less hydrophobic domains were located about 100 amino acids downstream and upstream from the N and C termini, respectively (FIG. 6).

Example 2 Phylogenetic Analysis

An unrooted phylogenetic tree of the PiELO1 and several functionally characterized PUFA elongases was constructed to identify their functional and phylogenetic relationships by the neighbor-joining program in MEGA4. According to FIG. 7 one can see that PiELO1 falls into a group of PUFA elongases of lower eukaryotes. Although the group contains mostly PUFA elongases with Δ6 activity, some Δ5 elongases, e.g., that of M. polymorpha and Leishmania infantum, are more related to Δ6 elongases of lower eukaryotes than to Δ5 elongases of higher eukaryotes. PiELO1 makes a closely related subgroup with OtELO1, MpELO1, MpELO2 and PpELO1, the OtELO1 being the closest one.

Functional Expression of PiELO1 In S. Cerevisiae

To characterize the enzymatic activity of PiELO1, the pYES2 plasmid containing the PiELO1 ORF downstream of the GAL1 promoter was transformed into S. cerevisiae. The PiELO1 was expressed in the presence of the Δ6 PUFA elongase substrates, 18:3ω6 (γ-linolenic acid, GLA) and 18:4ω3 (stearidonic acid, STA). GC analysis of the FAMEs of transformed yeast cells showed that PiELO1 elongated GLA and STA, converting them into dihomo-γ-linoleic acid (DGLA, 20:3ω6) and eicosatetraenoic acid (20:4ω3), respectively (FIG. 8). The yeast cells harboring the empty vector alone did not demonstrate any elongation activity on the added substrates, confirming that the PiELO1 encoded enzyme has a Δ6 PUFA elongase activity. Feeding the PiELO1 transformants with the ω6 fatty acids, LA and ARA, did not result in their elongation (not shown).

Real-time quantitative PCR was performed to quantitate the alterations in expression levels of the Δ6 PiELO1 in P. incisa cells under nitrogen starvation. The expression levels of the genes under nitrogen starvation were measured and normalized to the expression level of the endogenous control gene 18S SSU rRNA. The fold change in the expression level of the target genes in P. incisa cells grown for 3, 7 and 14 d on N-free medium was calculated relative to the expression level of the target genes in the log phase (time 0). The results showed that during nitrogen starvation the mRNA of the PiELO1 gene was induced to its highest level at day 3 (14 fold increase over time 0), decreasing thereafter to a level still higher than that of day 0 (FIG. 9). After 7 and 14 d, the expression level of the PiELO1 gene was still 7.5 and 4.3 fold higher, respectively. The level of expression of the PiELO1 gene correlated with the increase in the share of ARA and the C20/(C16+C18) elongation ratio (Table 7). The share of the elongation product, DGLA, increased sharply at day 3 (50% increase over time 0) and decreased thereafter.

TABLE 7 Major fatty acid composition of P. incisa cells grown under N-starvation Time Fatty acid composition (% of total fatty acids) Elo. (days) 16:0 16:1 16:2 16:3 18:0 18:1 18:2 18:3ω6 18:3ω3 20:3ω6 20:4ω6 20:5ω3 ratio^(a) 0 19.1 5.6 4.1 2.9 3.1 9.1 20.1 1.2 6.0 0.5 23.0 0.7 0.34 3 12.7 2.3 1.5 1.9 3.8 15.2 13.5 1.6 2.0 0.9 39.7 0.6 0.74 7 10.7 1.0 0.6 1.1 3.5 14.9 10.0 1.1 0.9 1.0 50.0 0.5 1.10 14 9.0 0.2 0.3 0.8 3.1 13.4 8.8 0.9 0.6 0.9 56.9 0.6 1.44 ^(a)Elongation ratio, C20/(C18 + C16)

The capacity of P. incisa to accumulate large quantities of ARA-rich TAG under nitrogen starvation, suggested that it would be of great interest to study its genes and enzymes involved in the accumulation of VLC-PUFA. In the present work, P. incisa Δ12, Δ6, and Δ5 desaturases were cloned and studied, which in conjunction with a recently cloned Δ6 specific PUFA elongase [U. Iskandarov, I. Khozin-Goldberg, R. Ofir, Z. Cohen, Cloning and Characterization of the Δ6 Polyunsaturated Fatty Acid Elongase from the Green Microalga Parietochloris incisa, Lipids 44 (2009) 545-554.], represent a set of P. incisa genes involved in the biosynthesis of ARA. U. Iskandarov et al., 2009 is incorporated by reference as if fully set forth herein.

The his-boxes of Δ12, Δ6 and Δ5 desaturases including PiDes12, PiDes6, and PiDes5 are detailed in Table 8.

TABLE 8 Conserved histidine rich motifs of Δ12, Δ6, and Δ5 desaturases Des Δ12 HECxH HxxHH HxxHH Des Δ6 HD_((E))xxH HxxHH QxxHH Des Δ5 HDxxH QHxxxHH QxxHH

Notably, cysteine (C) in the first his-box and the first histidine (H) in the third his-boxes, respectively, are conserved only in Δ12 desaturases. The second residue in the first his-box of the all three types of desaturases is acidic; in Δ6 and Δ5 desaturases it is mostly aspartic acid (D), and in Δ12 desaturases mostly glutamic acid (E). This indicates the importance of an acidic residue at this position for desaturation. Similarly to other Δ6 and Δ5 desaturases glutamine (Q) is found in the third his-box of PiDes6 and PiDes5 (FIG. 1; Table 8) and in the second his-box of Δ5 desaturases. The replacement of the H residue with Q in the third his-box of Δ6 and Δ5 desaturases points to the role of Q in PUFA desaturation. Indeed, replacing this Q with histidine or isoleucine eliminated the enzyme activity of the recombinant Δ6 desaturase in yeast cells. Glutamine was also found to be highly conserved in the third his-box of the Δ4 desaturases Pavlova lutheri (AY332747), Euglena gracilis (AY278558), and Thraustochytrium sp. (AF489589).

Heterologous expression of PiDes6 and PiDes5 in yeast cells confirmed their Δ6 and Δ5 activity by conversion of supplemented fatty acids to the corresponding desaturation products. PiDes12 demonstrated very low desaturation activity, which could not be enhanced by the 5′ modification of the inserted sequence. A similar low activity in yeast was also demonstrated in some cases, such as for Δ5 and Δ12 desaturases of O. tauri and Chlorella vulgaris NJ-7, respectively.

PiDes6 and PiDes5 desaturated both ω3 and ω6 fatty acids with similar efficiency (FIG. 3; Table 4). Various results concerning ω3/ω6 substrate preference were reported for functionally characterized Δ6 and Δ5 desaturases from different organisms that were expressed in yeast. A front-end PiDes5 desaturated its principal substrate 20:3ω6 as well as 20:4ω3; in addition, non-methylene interrupted fatty acids were also produced as a result of its activity on 20:3ω3, and on both endogenous and exogenous 18:1, but with lower efficiency. PiDes5 produced 18:2^(Δ5,9) from 18:1 but was more active when 18:1 was exogenously supplied. CrDES did insert Δ5 double bond on both 18:1 and 18:2 producing the non-methylene interrupted 18:2^(Δ5,9) and 18:3^(Δ5,9,12), while adding a Δ7 double bond to 20:2ω6 and 20:30ω. Apparently, in addition to the fatty acid chain length, the location and number of double bond, and the form of the substrate (lipid- or CoA bound) are also crucial for Δ5 desaturation.

PiDes6 desaturated neither the yeast major monounsaturated fatty acids nor the exogenously supplied 18:1. PiDes6 did not act on 20:3ω3, indicating that it is specific for Δ9 C18 PUFA. It appears that not only the organisms being transformed, but also the gene origin, determine the substrate specificity of the recombinant Δ6 and Δ5 desaturase. Functional characterization of PiDes6 and PiDes5 confirmed the previously reported substrate specificities of these desaturases which were generally restricted to C18 and C20 substrates, respectively.

In P. incisa it was shown that PC and DGTS are used for lipid-linked C18 Δ6 desaturation whereas mostly PE is used for C20 Δ5 desaturation. PiDes5 featured higher substrate conversion rate in comparison to PiDes6. A relatively fast emergence of substantial percentage of ARA (10.6% conversion after 3 h of feeding) pursued us to study ARA distribution in individual lipid classes of the transformed yeast (24 h of feeding). ARA was detected in all analyzed phospho- and neutral lipid classes of S. cerevisiae expressing PiDes5 (Table 5). Similar conversion percentages were determined in all analyzed phospholipids, however, ARA distribution showed preference for the major phospholipids, PC, followed by PE. In P. incisa, PE was found to be the main site for lipid-linked Δ5 desaturation [C. Bigogno, I. Khozin-Goldberg, D. Adlerstein, Z. Cohen, Biosynthesis of arachidonic acid in the oleaginous microalga Parietochloris incisa (Chlorophyceae): Radiolabeling studies, Lipids 37 (2002) 209-216], while PC, a major Δ6 acyl lipid desaturation substrate in this organism, was assumed to be utilized for Δ5 desaturation, too.

The quantitative RT-PCR results revealed that the gene expression levels of PiDes12, PiDes6, and PiDes5 followed a similar pattern during the course of nitrogen starvation. The major transcriptional activation of the all three desaturases occurred on day 3 coinciding with a sharp rise in the percentage of ARA, which almost doubled (FIG. 4, Table 6). The same expression pattern featured the P. incisa Δ6 PUFA elongase, however, at lower level. It was shown in radiolabeling and inhibitor studies, that ARA biosynthesis in P. incisa follows the ω6 pathway. The concerted transcriptional activation of the PiDes12, PiDes6, PiDes5 and PiELO1 genes was accompanied by an increase in the percent share of 18:1, a main chloroplast-derived fatty acid exported to ER and substrate of Δ12 desaturase. High expression of ARA biosynthetic genes was accompanied by enhanced Δ5 and Δ6 desaturations (Table 6).

In conclusion, the Δ12, Δ6 and Δ5 fatty acid desaturases involved in ARA biosynthesis in P. incisa were identified and functionally characterized. The corresponding ORFs PiDes12, PiDes6, and PiDes5, expressed in yeast confirmed their favorable enzymatic activity. Nitrogen starvation led to an increased transcription of the cloned genes reaching maximum on day 3 and enhanced accumulation of ARA thereafter. Understanding the mechanisms underlying gene transcription regulation in metabolic pathways and characteristics of enzymes involved in ARA and lipid biosynthesis in P. incisa is a prerequisite for manipulating algal species to produce sustainable oils of pharmaceutical and neutraceutical values.

A cDNA (PiELO1) of an elongase encoding for a deduced protein was isolated from P. incisa, structurally similar to 46 PUFA elongase gene products from microalgae, lower plants and fungi (FIG. 5). The deduced amino acid sequence of the PiELO1 ORF was about 50% identical to that of 46 elongases from the liverwort M. polymorpha (AAT85662), the green marine microalga O. tauri (AAV67797) and the moss P. patens (AAL84174). In similarity to recently cloned PUFA elongases, the predicted protein is highly hydrophobic and has two strongly hydrophobic transmembrane regions, the first one located about 50 amino acids downstream of the N-terminus and the second one in the vicinity of the C-terminus. The PiELO1 sequence was identified in a C-terminal lysine-rich motif, important for the endoplamic reticulum targeting, as well as four conserved motifs FYxSKxxEFxDT, QxxxLHVYHHxxI, NSxxHVxMYxYY and TxxQxxQF, including a highly conserved histidine box suggested to be functionally important for PUFA elongation (FIG. 5). These conserved motifs were not found in other classes of plant microsomal elongases, β ketoacyl CoA synthases and fatty acid elongases (FAE) involved in extraplastidial elongation of saturated and monounsaturated fatty acids. A variant histidine box QAFHH with three replacements in C18-Δ9-PUFA elongase IgASE1 from I. galbana is thought to be important for enzymatic activity rather then for substrate specificity.

PiELO1 is another example of a single step Δ6 PUFA elongases cloned from an algal species. Similarly to GLELO of M. alpina, PiELO1 prefers the Δ6 C18 PUFA substrates, GLA and STA. Only these Δ6 fatty acids were, when exogenously added, elongated to the respective products by S. cerevisiae cells transformed with PiELO1 (FIG. 8). Transformation of a higher plant so as to render it to produce Δ6 PUFA requires that the elongase used will have a high selectivity for Δ6 PUFA, thereby reducing the appearance of side products in the transformed plant. Bifunctional invertebrate PUFA elongases with both Δ6 and Δ5 activities (OmELO, XiELO, and CiELO) are less desirable in plant transformations.

Phylogenetic analysis showed (FIG. 6) that the PUFA elongases are not strictly divided according to their substrate specificity. The Δ6 elongases of algal (OtELO1, TpELO1, PiELO1) and moss (PpELO1) origin are functionally restricted to the elongation of Δ6-C18-PUFAs, however these elongases are placed in separate groups on the phylogenetic tree (FIG. 7). PiELO1 is closely related to OtELO1 isolated from a chloropyte and a lower plant rather than to ELO1 genes isolated from a diatom, although both are specific for the elongation of Δ6-C18-PUFAs (FIG. 7). PiELO1 is highly similar to and is placed in the same group with both Δ6 and Δ5 elongases of the liverwort M. polymorpha. Kajikawa et al. suggested that MpELO2, a Δ5 elongase, is likely to have originated through gene duplication of the MpELO1 gene. The algal Δ5 PUFA elongases, OtELO2, TpELO2 and the P. salina ELO1 are more likely to share a common branch with the mammalian and animal Δ5 PUFA elongases, OmELO and HsELO2, while they are also similar to bifunctional PUFA elongases such as CiELO1/2.

Quantitative real timd PCR studies revealed that the expression level of the PiELO1 gene was up regulated during the time course of N-starvation (FIG. 9). Nitrogen starvation led to a continuous increase in the share of ARA and the C20/(C16+C18) elongation ratio (Table 7). However, a major transcriptional activation of PiELO1 which occurred on day 3 (14-fold increase in transcript level) coincided with the steep rise in AA accumulation and elongation ratio (Table 7). The increase in PiELO1 transcription level followed by enhanced biosynthesis of ARA may be interpreted as an increase in PiELO1 enzyme level and/or enzymatic activity. The importance of the transcriptional activation of PiELO1 is supported by the fact that PUFA elongase was the only ARA biosynthesis related gene that was obtained from the subtractive library.

The significance of the coordinated transcription and action of desaturases and elongases in ARA biosynthesis in P. incisa is yet to be elucidated. Possibly, the elongation of GLA by PiELO1 could be rate-limiting in ARA biosynthesis as it is in M. alpina. Abbadi et al. (2004) speculated that in transgenic plants modified with VLC-PUFA biosynthesis genes, substrate availability rather than enzymatic activity is rate-limiting in the Δ6 elongation of PUFA. 

1. An isolated protein comprising, an amino acid sequence set forth in SEQ ED NO:
 1. 2. A composition comprising the protein of claim
 1. 3. An isolated protein comprising, an amino acid sequence set forth in SEQ ID NO:
 2. 4. A composition comprising the protein of claim
 3. 5. An isolated protein comprising, an amino acid sequence set forth in SEQ ID NO:
 3. 6. A composition comprising the protein of claim
 5. 7. An isolated polynucleotide comprising a coding portion encoding the protein of claim
 1. 8. The isolated polynucleotide of claim 7, wherein said coding portion comprises a nucleic acid sequence set forth in SEQ ID NO:
 4. 9. An isolated polynucleotide comprising a coding portion encoding the protein of claim
 3. 10. The isolated polynucleotide of claim 9, wherein said coding portion comprises a nucleic acid sequence set forth in SEQ ID NO:
 5. 11. An isolated polynucleotide comprising a coding portion encoding the protein of claim
 5. 12. The isolated polynucleotide of claim 11, wherein said coding portion comprises a nucleic acid sequence set forth in SEQ ID NO:
 6. 13. An expression vector comprising the polynucleotide of claim
 7. 14. An expression vector comprising the polynucleotide of claim
 9. 15. An expression vector comprising the polynucleotide of claim
 11. 16. A cell comprising the expression vector of claim
 13. 17. A cell comprising the expression vector of claim
 14. 18. A cell comprising the expression vector of claim
 15. 19. A transgenic plant, a transgenic seed, or a transgenic alga transformed by a polynucleotide of claim
 7. 20. A transgenic plant, a transgenic seed, or a transgenic alga transformed by a polynucleotide of claim
 9. 21. A transgenic plant, a transgenic seed, or a transgenic alga transformed by a polynucleotide of claim
 11. 22. A transgenic seed, produced by a transgenic plant transformed by a polynucleotide of claim
 7. 23. A transgenic seed, produced by a transgenic plant transformed by a polynucleotide of claim
 9. 24. A transgenic seed, produced by a transgenic plant transformed by a polynucleotide of claim
 11. 25. A method of producing very long-chain polyunsaturated fatty acid (VLC-PUFA) in a plant, a plant cell, or an alga comprising the step of transforming a plant, a plant cell, or an alga with a polynucleotide of claim 7, thereby producing a VLC-PUFA in a plant, a plant cell, or an alga.
 26. A method of producing very long-chain polyunsaturated fatty acid (VLC-PUFA) in a plant, a plant cell, or an alga, comprising the step of transforming a plant, a plant cell, or an alga with a polynucleotide of claim 9, thereby producing a VLC-PUFA in a plant, a plant cell, or an alga.
 27. A method of producing very long-chain polyunsaturated fatty acid (VLC-PUFA) in a plant, a plant cell, or an alga, comprising the step of transforming a plant, a plant cell, or an alga with a polynucleotide of claim 11, thereby producing a VLC-PUFA in a plant, a plant cell, or an alga.
 28. The method of claim 25, wherein said plant, said plant cell, or said alga comprises linoleic acid (LA; 18:2ω6), α-linolenic acid (ALA; 18:3ω3), oleic acid (18:1), dihomo-gamma-linolenic acid (20:3ω6), phosphatidylcholine (PC), diacylglyceroltrimethylhomoserine (DGTS), phosphatidylethanolamine (PE), or any combination thereof.
 29. The method of claim 25, wherein said VLC-PUFA is eicosapentaenoic acid (EPA, 20:5ω3), docosahexaenoic acid (DHA, 22:6ω3), dihomo-gamma-linolenic acid (DGLA), or arachidonic acid (ARA, 20:4ω6)
 30. The method of claim 25, wherein said plant, said plant cell, or said alga is grown under oleogenic conditions, under nitrogen starvation conditions, or a combination thereof.
 31. The method of claim 25, wherein said producing very long-chain polyunsaturated fatty acid (VLC-PUFA) is enhancing oil storage, arachidonic acid accumulation, eicosapentaenoic acid accumulation, docosahexaenoic acid accumulation, dihomo-gamma-linolenic acid accumulation, or a combination thereof.
 32. The method of claim 25, further comprising the a step of transforming said plant, said plant cell, or said alga with a polynucleotide of claim 9, a polynucleotide of claim 11, a polynucleotide encoding a PUFA-specific elongase, or any combination thereof.
 33. The method of claim 26, further comprising the a step of transforming said plant, said plant cell, or said alga with a polynucleotide of claim 7, a polynucleotide of claim 11 , a polynucleotide encoding a PUFA-specific elongase, or any combination thereof.
 34. The method of claim 27, further comprising the a step of transforming said plant, said plant cell, or said alga with a polynucleotide of claim 7, a polynucleotide of claim 9, a polynucleotide encoding a PUFA-specific elongase, or any combination thereof.
 35. The method of claim 26, wherein said plant, said plant cell, or said alga comprises linoleic acid (LA; 18:2ω6), α-linolenic acid (ALA; 18:3ω3), oleic acid (18:1), dihomo-gamma-linolenic acid (20:3ω6), phosphatidylcholine (PC), diacylglyceroltrimethylhomoserine (DGTS), phosphatidylethanolamine (PE), or any combination thereof.
 36. The method of claim 26, wherein said VLC-PUFA is eicosapentaenoic acid (EPA, 20:5ω3), docosahexaenoic acid (DHA, 22:6ω3), dihomo-gamma-linolenic acid (DGLA), or arachidonic acid (ARA, 20:4ω6)
 37. The method of claim 26, wherein said plant, said plant cell, or said alga is grown under oleogenic conditions, under nitrogen starvation conditions, or a combination thereof.
 38. The method of claim 26, wherein said producing very long-chain polyunsaturated fatty acid (VLC-PUFA) is enhancing oil storage, arachidonic acid accumulation, eicosapentaenoic acid accumulation, docosahexaenoic acid accumulation, dihomo-gamma-linolenic acid accumulation, or a combination thereof.
 39. The method of claim 27, wherein said plant, said plant cell, or said alga comprises linoleic acid (LA; 18:2ω6), a-linolenic acid (ALA; 18:3ω3), oleic acid (18:1), dihomo-gamma-linolenic acid (20:3ω6), phosphatidylcholine (PC), diacylglyceroltrimethylhomoserine (DGTS), phosphatidylethanolamine (PE), or any combination thereof.
 40. The method of claim 27, wherein said VLC-PUFA is eicosapentaenoic acid (EPA, 20:5ω3), docosahexaenoic acid (DHA, 22:6ω3), dihomo-gamma-linolenic acid (DGLA), or arachidonic acid (ARA, 20:4ω6)
 41. The method of claim 27, wherein said plant, said plant cell, or said alga is grown under oleogenic conditions, under nitrogen starvation conditions, or a combination thereof.
 42. The method of claim 27, wherein said producing very long-chain polyunsaturated fatty acid (VLC-PUFA) is enhancing oil storage, arachidonic acid accumulation, eicosapentaenoic acid accumulation, docosahexaenoic acid accumulation, dihomo-gamma-linolenic acid accumulation, or a combination thereof. 